(CMDCP) Certified Medical Device Compliance Professional™

View Required Courses Certification FAQs

About the Certified Medical Device Compliance Certification Program

CfPIE’s Certified Medical Device Compliance Professional (CMDCP) certification program offers medical device compliance training and a certification opportunity to professionals responsible for compliance. The CMDCP certification program is available for individuals in the United States, Europe, Canada, Australia and Middle Eastern countries. Full List of Countries where we offer Pharma & Biotech and Medical Device Courses.

The CMDCP program is designed to give industry personnel the robust compliance training needed to advance their careers and satisfy regulatory training requirements. CfPIE medical devices compliance programs cover topics from quality and manufacturing concerns to product design, clinical trials, validation and regulatory filings.

With CfPIE you can be sure to select the compliance certification program path that best suits your current responsibilities and career goals.

Contact a Training Advisor

We offer on-site pharmaceutical training and life science certification programs for organizations with 10 or more employees enrolling. Call us today at 1-610-648-7550 or Contact a Training Advisor.

Proceed To Required Courses Certification FAQs

Certification Requirements:

Choose 3 Core Courses from any of the courses listed below.
Choose 1 Elective Course (Can be a core course or any course listed at: Courses by Title)

Auditing and Qualifying Suppliers and Vendors Biostatistics for Non-Statisticians Computer System Validation Effective Document Management for Pharma, Biotech & Medical Device Ethics in Research - Values for Responsible Conduct of Research FDA Inspections – What Regulators Expect & How to Prepare Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Introduction to Medical Combination Products Introduction to Statistical Analysis of Laboratory Data Marketing & Advertising of Pharmaceutical & Medical Devices

Medical Device Process Validation Training for Professionals Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Overview of FDA Regulatory Compliance for Medical Devices Overview of the New EU Medical Devices Regulations: MDR, IVDR, CE Mark and Compliance, QMS Fundamentals Pharmaceutical Production Batch Record Review Preparation of FDA Submissions and Communicating with the FDA Technical Writing for Pharma, Biotech and Med Devices US Medical Device & Quality System Regulations - Design Controls & Validation Writing Effective SOP and Other Process Documents

Certification Program Discounts

If you have 10 or more employees that would benefit from this certification program, we can offer complete program tracks on-site at your facility. For more information call us at 1-610-648-7550 or contact us.

Pharma & Biotech Courses

Medical Device Courses

Skin & Cosmetics Courses

Since 2006 CfPIE has