Inspire and influence your team members to achieve your goals as a team!
Chris DeVany
Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation
Carolyn Troiano
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.
Mark Schwartz
This seminar will begin with a general discussion of technical writing and its role within the life sciences.
Charles H. Paul
This 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house
Brian Tuttle
You Have Literally Been Cheated Your Entire Life And It's Not Your Fault!
Paul J. Cline
Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.
Chris DeVany
The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."
Diane L Dee
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.
Elaine Eisenbeisz
The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
Joy McElroy
Human error is known to be the primary cause of quality and production losses in many industries.
Ginette Collazo
Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical
Michael Esposito
The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule
Jim Sheldon Dean
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.
Robert J. Russell
One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean Union requirements.
John E Lincoln
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.
William Mack Copeland
This 6-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process
Susanne Manz
Today's workforce is experiencing high turnover and disengaged employees.
Tonia Morris
In this seminar you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.
Tom Fragale
There is a broad need to understand the impact of global influenza outbreaks for the food industry.
Gina Reo
The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.
Karla Brandau
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.
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.
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
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.
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.
The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.
In this seminar you will learn how to take your raw data, and create meaningful reports using the powerful tools in Microsoft Excel.
This 6-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process
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 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house
There is a broad need to understand the impact of global influenza outbreaks for the food industry.
You Have Literally Been Cheated Your Entire Life And It's Not Your Fault!
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.
Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.
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.
Human error is known to be the primary cause of quality and production losses in many industries.
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.
The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical
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.
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.
Today's workforce is experiencing high turnover and disengaged employees.
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.
The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.
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 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.
