Statistical Process Control charts have been called the Voice of the Process. Progressive manufacturers utilize control charts to "listen" to their processes so that potentially harmful changes will be quickly detected and rectified.

This 6-hour virtual seminar includes a presentation of the steps and techniques used to quantify variability in manufacturing processes, and to assure quality products.

This 6-hour virtual seminar includes a presentation of the steps and techniques used to quantify variability in manufacturing processes, and to assure quality products.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

This webinar will focus on the key areas that are most important for protecting the validity of data that is regulated by FDA, and is typically housed electronically in computer systems.

Statistics is a useful decision making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on development of a drug or procedure, it is imperative that decision makers understand the theory and application of statistics.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited. The CTD has improved the regulatory review processes and enabled implementation of good review practices. The eCTD has increased efficiency for reviewers and improved submission times. Beginning in May 2017, the eCTD will be required in the US for all marketing applications.

Early clinical trials are conducted to establish initial safety of a drug. The studies are generally in small number of healthy subjects and use lower doses of the drug product. Therefore, only small amounts of investigational material are required. In order to not undertake substantial costs and to reduce regulatory burden during these early stages, the FDA has established guidelines to allow early stage investigational products to be manufactured under less stringent GMPs.

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable.

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood the extent of the commitments we make when we write an SOP or how the writing of the SOP can have a positive or negative impact on training or job performance.

Importing FDA regulated products requires careful planning before you even start. Registration, product compliance, record and data submission must be exactly correct or your product will be detained.

Human error is known to be the primary cause of quality and production losses in many industries.

This seminar will demonstrate how Covered Entities and Business Associates can comply calmly, confidently and completely with the HIPAA Rules.

This seminar will demonstrate how Covered Entities and Business Associates can comply calmly, confidently and completely with the HIPAA Rules.

This six-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more. It will also address major changes under the Omnibus Rule, Trump administration, and any other applicable updates for 2018 and beyond.

This 6-hour webinar takes the participants through HIPAA compliance from start to compliance.

This six-hour seminar will be going into great detail regarding you practice or business information technology and how it relates to

This 6 -hour virtual seminar will help you to develop a Quality Management System (QMS) for Medical Device Companies.

This course is appropriate for beginner and experienced person alike.

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.

This course will provide the attendees with more detailed experience on validation / 21 CFR 11 compliance of a computer system

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December

This 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house

This virtual seminar will address those project management critical tasks within each project phase that must

This 6-hour virtual seminar includes a presentation of the steps and techniques used to quantify variability in manufacturing processes, and to assure quality products.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability

This 6-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process

This course covers the requirements for conducting Clinical Studies across the EU via the requirements of

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

The world is swimming in data yet raw data is mostly useless without methods to turn this data into useful

As more and more students are being identified with Autism Spectrum Disorder, educators, parents and therapists are looking for the best practices to help these students experience success in the school and home setting as well as supports for communication, social skills and behavior.

Human error is known to be the primary cause of quality and production losses in many industries.

Statistics is a useful decision making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on development of a drug or procedure, it is imperative that decision makers understand the theory and application of statistics.

This six-hour seminar will be going into great detail regarding you practice or business information technology and how it relates to the HIPAA/HITECH Security Rule and securing PHI in transmission.

Gain the insights and skills to know where your business stands today and where it's heading tomorrow.

This webinar will focus on the key areas that are most important for protecting the validity of data that is regulated by FDA, and is typically housed electronically in computer systems.

In 2012, the Commission adopted a package of measures on innovation in health.

This webinar will begin with a general discussion of technical writing and its role within the life sciences.

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics

This webinar will aim at understanding and scoping out various phases of Qualification activities that

The impact of Data Integrity issues on a regulated company can be significant: it can result in recalls of products, warning or untitled letters, import alerts, injunctions, seizures, legal action, etc.

Thorough Understanding of HIPAA Rules

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue.

The world is swimming in data yet raw data is mostly useless without methods to turn this data

This day long webinar aims to train practitioners who already own a private practice are just getting started

As more and more students are being identified with Autism Spectrum Disorder.

Professionals are under more stress than ever evidenced by increases in demand for better services that are more efficient and thorough, higher costs, reduced staffing, and diminishing resources.

Human error is known to be the primary cause of quality and production losses in many industries.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES)

The session begins with overview of the HIPAA regulations and then continues with presentation.

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform.

The FDA and U.S. Customs and Border Protection are using new import requirements.

GxP Regulated companies are dependent on validated GxP computerized applications to conduct their day to day operations.

Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy subjects and use lower doses of the drug product.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Statistics is a useful decision making tool in the clinical research arena. When working in a field where a p-value

Too many healthcare organizations believe they have HIPAA compliance under control, but recent HIPAA Compliance Audits

This seminar will demonstrate how Covered Entities and Business Associates can comply calmly

When working or living with a child/adolescent with an Autism Spectrum Disorder, meltdowns may occur that

The world is swimming in data yet raw data is mostly useless without methods to turn this data

This 6-hour webinar takes the participants through HIPAA compliance from start to compliance.

Legal compliance can get confusing when some legal regulations seemingly overlap or even seem almost contradictory to implement.

This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated.

When an employer receives an allegation of workplace harassment, taking prompt and appropriate action is the employer's legal responsibility.

The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.

This webinar will begin with a general discussion of technical writing and its role within the life sciences.

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

This Virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this seminar is for you.

This 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics

The world is swimming in data yet raw data is mostly useless without methods to turn this data

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Human error is known to be the primary cause of quality and production losses in many industries.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES).

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

The session begins with overview of the HIPAA regulations and then continues with presentation

This Virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this seminar is for you.

Today's workforce is experiencing high turnover and disengaged employees.

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018.

This 6-Hour Virtual Seminar will get into the fine details of what we need to do and how to do it.

Knowing what to do in increasingly complicated employee situations can be difficult for even seasoned Managers and Supervisors, especially if a Supervisor has never had training.

Six Sigma is a powerfully dynamic approach to process improvement in order to do things better, faster, and at a lower cost.

Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy

In 2012, the Commission adopted a package of measures on innovation in health.

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated

Importing FDA regulated products requires careful planning before you even start. Registration, product compliance

Gain the insights and skills to know where your business stands today and where it's heading tomorrow.

When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data.

When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability

This webinar will begin with a general discussion of technical writing and its role within the life sciences.

The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.

This webinar will focus on the key areas that are most important for protecting the validity of data that is regulated by FDA

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product

This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated with

Inspire and influence your team members to achieve your goals as a team!

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December

This webinar will begin with a general discussion of technical writing and its role within the life sciences.

There are two phases to this topic. The first is auditing itself. Good audits are well structured.

In this program, we will review the physician anti-referral laws (Stark I and II), provide an in-depth discussion of physician employment contracting, review the relevant Stark exceptions and discuss how physician compensation models can be in compliance with the Stark prohibitions.

Importing FDA regulated products requires careful planning before you even start. Registration, product compliance

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution

Early clinical trials are conducted to establish initial safety of a drug.

Despite best efforts, serious quality issues resulting in a recall can occur.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation.

Legal compliance can get confusing when some legal regulations seemingly overlap or even seem almost contradictory to implement.

Human error is known to be the primary cause of quality and production losses in many industries.

Importing FDA regulated products requires careful planning before you even start. Registration, product compliance

This course is appropriate for beginner and experienced person alike.

Statistical Process Control charts have been called the Voice of the Process. Progressive manufacturers utilize control charts to "listen" to their processes so that potentially harmful changes will be quickly detected and rectified.

There are two phases to this topic. The first is auditing itself. Good audits are well structured.

The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.

This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated with

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy

The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product.

Gain the insights and skills to know where your business stands today and where it's heading tomorrow.

The world is swimming in data yet raw data is mostly useless without methods to turn this data into useful

In 2012, the Commission adopted a package of measures on innovation in health.

If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue.

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

Importing FDA regulated products requires careful planning before you even start. Registration, product compliance

This webinar concentrates on five areas of wage and hour law:

One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean Union requirements.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

This 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

Statistical Process Control charts have been called the Voice of the Process. Progressive manufacturers utilize control charts to "listen" to their processes so that potentially harmful changes will be quickly detected and rectified.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

This seminar provides Professionals working in this area with:

A strong credit culture:

Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy subjects and use lower doses of the drug product.

Human error is known to be the primary cause of quality and production losses in many industries.

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

Gain the insights and skills to know where your business stands today and where it's heading tomorrow.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical

This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics).

The world is swimming in data yet raw data is mostly useless without methods to turn this data into useful and actionable information.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.

Statistics is a useful decision making tool in the clinical research arena.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan.

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

Do you know the common mistakes made by employers that result in audits?

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

FDA’s import and export programs are complex, detailed and undergo changes without notice to the public.

One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean Union requirements.

In this webinar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

This seminar concentrates on five areas of wage and hour law:

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

Today's workforce is experiencing high turnover and disengaged employees.

In this webinar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December of 2017 respectively

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."

The use of statistics in clinical trials insures a valid and robust study which minimizes bias in assessing the efficacy of new drug treatment or medical devices.

Statistical Process Control charts have been called the Voice of the Process. Progressive manufacturers utilize control charts to "listen" to their processes so that potentially harmful changes will be quickly detected and rectified.

Do you know the common mistakes made by employers that result in audits?

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

This 6-hour virtual seminar includes a presentation of the steps and techniques used to quantify variability in manufacturing

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

Six Sigma is a powerfully dynamic approach to process improvement in order to do things better, faster, and at a lower cost.

In this webinar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

Do you know the common mistakes made by employers that result in audits?

This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean Union requirements.

In this webinar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

Do you know the common mistakes made by employers that result in audits?

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

In this seminar you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

Human error is known to be the primary cause of quality and production losses in many industries.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean Union requirements.

This 6-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process

The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

Design Control is considered a critical process by the FDA.

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

In this seminar you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.

This 6-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process

In this seminar you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Inspire and influence your team members to achieve your goals as a team!

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

In this webinar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

Six Sigma is a powerfully dynamic approach to process improvement in order to do things better, faster, and at a lower cost.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”). These Old, Outdated Ideas Will Not Take You Or Your Business To The Next Level.

Do you know the common mistakes made by employers that result in audits? Although agencies will tell you that you were selected "randomly;" the truth is there are one or more red flags that made you a target.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

Inspire and influence your team members to achieve your goals as a team!

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

This 4-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process

You Have Literally Been Cheated Your Entire Life And It's Not Your Fault!

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

Good leaders walk the talk, but they also write right. They know how to say in a few words what needs to be said in crisp, clear language.

This 4-Hour Virtual Seminar will get into the fine details of what we need to do and how to do it.

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Inspire and influence your team members to achieve your goals as a team!

The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."

This 6-hour virtual seminar includes a presentation of the steps and techniques used to quantify variability in manufacturing

This 4-hour webinar takes the participants through HIPAA compliance from start to compliance.

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical

This 4-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process

In this Seminar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

Do you know the common mistakes made by employers that result in audits?

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

Inspire and influence your team members to achieve your goals as a team!

The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."

Excel has a variety of tools like sorting, filtering, and subtotal to manage large lists of data, but if you need to analyze all that data and do it quickly, there's no better feature than a PivotTable. You can quickly create a compact summary report (based on tons of data) without needing to write complex formulas or rely on lengthy techniques.

The use of statistics in clinical trials insures a valid and robust study which minimizes bias in assessing the efficacy of new drug treatment or medical devices.

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule.

This 4-hour seminar takes the participants through HIPAA compliance from start to compliance.

One of our most popular seminars, continuously updated with the latest U.S. FDA and European Union requirements.

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. ("Belief Systems"). These Old, Outdated Ideas Will Not Take You Or Your Business To The Next Level.

This 4-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company.

This session will answer your questions on how to Attract, Retain and Engage Millennials

This highly interactive Seminar offers you and your team an array of practical tools to coach effectively in today’s work environment. You'll learn practical techniques for making your direct reports feel welcome, trust you to maintain confidence, to listen, and develop an Action Plan collaboratively with each f your team members, enhancing your overall team performance!

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

Inspire and influence your team members to achieve your goals as a team!

The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule.

One of our most popular seminars, continuously updated with the latest U.S. FDA and European Union requirements.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. ("Belief Systems"). These Old, Outdated Ideas Will Not Take You Or Your Business To The Next Level.

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable.

This 4-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company.

In this Seminar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

Today's workforce is experiencing high turnover and disengaged employees.

New supervisors will be ready to hit the ground running with the skills learned in this Webinar. Be ready to take on any challenge, be your best and put what you’ve learned into practice immediately.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”). These Old, Outdated Ideas Will Not Take You Or Your Business To The Next Level.

Inspire and influence your team members to achieve your goals as a team!

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

This highly interactive Seminar offers you and your team an array of practical tools to coach effectively in today’s work environment. You'll learn practical techniques for making your direct reports feel welcome, trust you to maintain confidence, to listen, and develop an Action Plan collaboratively with each f your team members, enhancing your overall team performance!

New supervisors will be ready to hit the ground running with the skills learned in this Webinar. Be ready to take on any challenge, be your best and put what you’ve learned into practice immediately.

Inspire and influence your team members to achieve your goals as a team!

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

This highly interactive Seminar offers you and your team an array of practical tools to coach effectively in today’s work environment. You'll learn practical techniques for making your direct reports feel welcome, trust you to maintain confidence, to listen, and develop an Action Plan collaboratively with each f your team members, enhancing your overall team performance!

New supervisors will be ready to hit the ground running with the skills learned in this Webinar. Be ready to take on any challenge, be your best and put what you’ve learned into practice immediately.

Inspire and influence your team members to achieve your goals as a team!

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

This highly interactive Seminar offers you and your team an array of practical tools to coach effectively in today’s work environment. You'll learn practical techniques for making your direct reports feel welcome, trust you to maintain confidence, to listen, and develop an Action Plan collaboratively with each f your team members, enhancing your overall team performance!

This 6-hour virtual seminar is an essential guide on how to create and implement an efficient and effective internal audit program. Internal Audit is a required part of an effective quality system. More importantly, it is an incredibly powerful tool to self-identify areas of non-compliance.

The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”). These Old, Outdated Ideas Will Not Take You Or Your Business To The Next Level.

In this seminar, you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.

The Seminar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject.

This 4-hour seminar takes the participants through HIPAA compliance from start to compliance.

This 4-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company.

New supervisors will be ready to hit the ground running with the skills learned in this Webinar. Be ready to take on any challenge, be your best and put what you’ve learned into practice immediately.

Inspire and influence your team members to achieve your goals as a team!

This highly interactive Seminar offers you and your team an array of practical tools to coach effectively in today’s work environment.

New supervisors will be ready to hit the ground running with the skills learned in this Webinar. Be ready to take on any challenge, be your best and put what you’ve learned into practice immediately.

Inspire and influence your team members to achieve your goals as a team!

This highly interactive Seminar offers you and your team an array of practical tools to coach effectively in today’s work environment.

This 4-Hour Virtual Seminar will get into the fine details of what we need to do and how to do it.

This 4-Hour Virtual Seminar will get into the fine details of what we need to do and how to do it.

This 6-Hour Virtual Seminar will get into the fine details of what we need to do and how to do it.

The Seminar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."

One of our most popular seminars, continuously updated with the latest U.S. FDA and European Union requirements.

Six Sigma is a powerfully dynamic approach to process improvement in order to do things better, faster, and at a lower cost.

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation.

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

Six Sigma is a powerfully dynamic approach to process improvement in order to do things better, faster, and at a lower cost.

Do you know the common mistakes made by employers that result in audits? Although agencies will tell you that you were selected "randomly;" the truth is there are one or more red flags that made you a target.

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.