The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."
Diane L Dee
Joy McElroy
This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics).
Robert J. Russell
In this program, we will review the physician anti-referral laws
William Mack Copeland
Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation.
Carolyn Troiano
The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
Joy McElroy
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
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.
Howard Baumgarten
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.
Peggy Berry
This seminar concentrates on five areas of wage and hour law:
Vicki M Lambert
This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018
Brian Tuttle
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.
Michael Esposito
The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
Joy McElroy
There are two phases to this topic.
Steven S Kuwahara
The world is swimming in data yet raw data is mostly useless without methods to turn this data into useful and actionable information.
Steven Wachs
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.
Charles H. Paul
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.
Danielle DeLucy
Human error is known to be the primary cause of quality and production losses in many industries.
Ginette Collazo
Early clinical trials are conducted to establish initial safety of a drug.
Peggy Berry
The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).
Paul J. Cline
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.
Rich Henriksen
The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).
Paul J. Cline
This seminar provides Professionals working in this area with:
Salma Michor
Statistics is a useful decision making tool in the clinical research arena.
Elaine Eisenbeisz
Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.
Chris DeVany
The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan.
Adriaan Fruijtier
A strong credit culture:
Dev Strischek
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.
Danielle DeLucy
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 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018
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.
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.
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.
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.
The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
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 employees are required to perform.
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.
Early clinical trials are conducted to establish initial safety of a drug.
This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics).
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.
There are two phases to this topic.
The world is swimming in data yet raw data is mostly useless without methods to turn this data into useful and actionable information.
This seminar concentrates on five areas of wage and hour law:
In this program, we will review the physician anti-referral laws
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 seminar provides Professionals working in this area with:
The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).
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.
A strong credit culture:
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 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 Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."
The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).
