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Regulatory Compliance Training Courses covering FDA Regulations from CfPA

Regulatory Compliance Training

Regulatory compliance training is important because regulatory agencies are legally entitled to conduct unannounced inspections if they believe there are suitable grounds for doing so.  Therefore, regulatory compliance training is needed so your organization can comply with the European (ICH) and US FDA regulations, specifications, and guidelines.

As the leader in continuing education and accredited technical training, The Center for Professional Advancement (CfPA) offers the most state-of-the-art, cutting-edge regulatory compliance training available. Our comprehensive curriculum of online and public courses run one- to five- days in length and include discussions, case studies, and group exercises which are taught by top industry leaders who share their knowledge in an enthusiastic, interactive manner. 


CfPA Regulatory Affairs Courses Pre-Approved By Regulatory Affairs Professionals Society (RAPS)
CfPA is a Regulatory Affairs Professionals Society (RAPS) RA Professional Development Portal provider. Select CfPA regulatory courses being offered this fall have been pre-approved by the Regulatory Affairs Professional Society (RAPS) which allows participants to be eligible for up to 12-16 credits from CfPA towards a participant’s RAC recertification, demonstrating that you have made a commitment to being a highly skilled and knowledgeable regulatory professional throughout the span of your career. This certification is provided by the Regulatory Affairs Professionals Society (RAPS), is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products. Select courses this fall have been pre-approved by RAPS.

Select courses have been pre-approved by RAPS. For a complete list of pre-approved courses-click here.

CfPA offers GxP regulatory compliance training covering the European (ICH) and US (FDA) regulations.  These GxP systems, aimed at providing reliable and quality work, are as follows:

Browse the Regulatory Compliance Training Courses listed below. CfPA can also bring any Regulatory Compliance Training Course to your location. Please click here for more information about our Client-Site Programs.

Course TitleScheduled
Auditing and Inspecting Preclinical Research for GLP Compliance 
Auditing for GMP Compliance 
cGMP and Quality Issues for Biopharmaceuticals 
cGMP Auditing - Strategies for Compliance 
cGMP for Pharmaceutical Quality Control Laboratory Personnel 
CMC Writing and Submission Strategies: A Global Regulatory Approach
Critical Process Cleaning and Cleaning Validation
Current Good Manufacturing Practice (cGMP) for Purchasing 
Current Good Tissue Practices (cGTPs) 
Design Control and Product Validation 
Developing Specifications for Drug Substances and Drug Products
Documentation Management and Control
Drug Regulatory Compliance/Drug Approval and Preapproval Inspection 
Early Stage Clinical Studies for Drugs and Devices 
Excipient GMPs 
FDA Drug Approval, Regulation and Compliance
GMP for Dietary Supplements
GMP/QSR/QSIT for Medical Devices 
Good Clinical Practices (GCP) 
Good Distribution Practices 
Good Laboratory Practices (GLP)
Non-Clinical Drug Safety Evaluation and Drug Development 
Pharmaceutical Quality Assurance and Control 
Preparing for and Surviving an FDA Inspection
Quality System 
Scale-Up and Post Approval Changes Guidelines (SUPAC & API Changes)
Selecting and Managing CROs 
Surviving an FDA Inspection -- FDA Inspections of Non-U.S. Sites 
Vendor and Contract Supplier Qualification 
Writing and Implementing Clinical Protocols  
Writing SOPs for cGMP Compliance 


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