Video Testimonials

What Your Colleagues are Saying About CfPIE

Medical Devices: EU Directives, CE Marking and ISO Standards Course

Meet Jonathan Lee, CfPIE's Course Director for “Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Course”. Jonathan gives a snapshot of the 2-day classroom course which introduces the Medical Device Directives (AIMD, MDD & IVDMDD), the meaning of the CE symbol and how & when to legitimately apply this mandatory mark of conformity.

Process Validation for Medical Devices Course

Meet Shannon Goodson, CfPIE's Course Director for "Process Validation for Medical Devices". Shannon gives a snapshot of the 3-day classroom course which focuses on how to comply with FDA and international regulations for validation protocols.

CfPIE Document Management Systems Course

In this video, both an attendee and Kay Monroe, a pharmaceutical industry veteran and the instructor of our “Effective Document Management Systems” course, discuss the benefits of our approach to training courses.

CfPIE Stability Programs Course

Meet John Geigert, CfPIE's Course Director for "Stability Programs for Determining Product Shelf Life – From Clinical Development to Market Approval". John gives a snapshot of the 2-day classroom course which focuses on the global requirements for stability testing, stability assignment, and shelf life assignment.

CfPIE Good Laboratory Practices (GLP) Course

Meet Ken Cleaver, CfPIE's Course Director for " Good Laboratory Practices (GLP) for Pre-Clinical Testing". Ken gives a snapshot of the 3-day classroom course which focuses on understanding the terminology, regulations and mandated practices for GLP testing and compliance.

Preparing the CMC Section for NDAs/INDs/CTDs Course

Meet Maria Geigel, CfPIE’s Course Director for “Preparing the CMC Section for NDAs/INDs/CTDs”. Maria gives a snapshot of the 2-day classroom course which focuses on the requirements related to drug substance starting materials, drug substance and drug product specifications, impurities, stability, and pharmaceutical development reports.

Good Manufacturing Practices (cGMP) Course

In this video, both an attendee and Steven A. Ostrove, Ph.D., a Bio-Pharmaceutical industry veteran and the instructor of our “Good Manufacturing Practices (cGMP)” course, discuss the benefits of our approach to training courses.

CfPIE Stability Programs Course

Hear from three attendees of CfPIE's 2-day "Stability Programs for Determining Product Shelf Life – From Clinical Development to Market Approval" course and learn, in their own words, how they expanded their knowledge on properly running a compliant stability program.

Good Manufacturing Practices (cGMP) Course

Hear from an attendee of CfPIE's 3-day "Good Manufacturing Practices (cGMP)" course and learn, in their own words, how they gained a fundamental knowledge of the basis of CGMP regulations, and the necessity of implementing them in daily operations.

Medical Devices: EU Directives, CE Marking and ISO Standards Course

Hear from an attendee of CfPIE's 2-day "Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications" course and learn, in their own words, how they expanded their knowledge on in marketing and supporting medical devices in the European Community.

Medical Devices: EU Directives, CE Marking and ISO Standards Course

Hear from an attendee of CfPIE's 2-day "Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications" course and learn, in their own words, how they expanded their knowledge on in marketing and supporting medical devices in the European Community.