The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."
This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics).
In this program, we will review the physician anti-referral laws
Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation.
The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
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.
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 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.
This seminar concentrates on five areas of wage and hour law:
This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018
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 objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
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 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.
Human error is known to be the primary cause of quality and production losses in many industries.
Early clinical trials are conducted to establish initial safety of a drug.
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.
The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).
This seminar provides Professionals working in this area with:
Statistics is a useful decision making tool in the clinical research arena.
Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.
The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan.
A strong credit culture:
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.
The first step in catapulting your career ahead of your competitors is fully to use Microsoft Outlook.
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”).