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

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

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

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 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.

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

This seminar provides Professionals working in this area with:

A strong credit culture:

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

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

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.

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

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

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.

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 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.

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

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.

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

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.

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

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

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 Exce

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.

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.

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.

When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable results in the receiving laboratory.

This 6 -hour virtual seminar will help you to develop a Quality Management System (QMS) for Medical Device Companies. A well-structured QMS meets the requirements of the Quality System Regulations and is both effective and efficient.

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.

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

This course is appropriate for beginner and experienced person alike.

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

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.

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.

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

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

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.

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

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

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

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

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

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.

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

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

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

This seminar provides Professionals working in this area with:

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

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

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

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.

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

This 6 -hour virtual seminar will help you to develop a Quality Management System (QMS) for Medical Device Companies. A well-structured QMS meets the requirements of the Quality System Regulations and is both effective and efficient.

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.

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

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.

GxP/GMP regulations are required to be used in regulated industries such as food, pharmaceutical, medical devices

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.

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? 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.

Much of what is taught in Sales courses today is Old B.S. ("Belief Systems") that just doesn't work for the Salesperson or Marketer anymore.

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

Design Control is considered a critical process by the FDA.

This webinar 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”).

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

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

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

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.