(CPVP) Certified Process Validation Professional™

View Required Courses Certification FAQs

About the Process Validation Certification Program

Our process validation training course is ideal for professionals in the Pharmaceutical, Medical Device, Biotech, Biopharmaceutical and Skin/Cosmetic industries who are tasked with process validation. The Certified Process Validation Professional (CPVP) 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.

Personnel involved in validation activities from product development through post-approval production concerns will find comprehensive insight on what regulators are looking for and become Certified Process Validation Professionals (CPVP) upon completion of the course.

This process validation training program requires completion of three of four core courses. Pharmaceutical personnel should select the Process Validation for Drugs and Biologics course and participants from Medical Device manufacturers should choose Process Validation for Medical Devices.

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)

ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Analytical Chemistry Principles for Pharmaceutical Scientists Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Auditing and Qualifying Suppliers and Vendors Best Practices for an Effective Cleaning Validation Program Biostatistics for Non-Statisticians Change Control - GMP Requirements and FDA Enforcement Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars Computer System Validation CRO, CDMO and Non-Clinical Vendor Management Fundamentals Effective Document Management for Pharma, Biotech & Medical Device Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Ethics in Research - Values for Responsible Conduct of Research FDA Inspections - What Regulators Expect and How to Prepare GMP Training for the QC Laboratory Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements Good Manufacturing Practices Training | GMP Course Human Error Prevention (HEP) - Risk Factors and Strategies

Integration of Risk Management Principles and Activities into the Pharmaceutical Quality System Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Introduction to Medical Combination Products Introduction to Statistical Analysis of Laboratory Data Introduction to Vaccines - CMC Regulatory and Quality Aspects Laboratory Equipment Validation and Qualification Lyophilization Technology - Application of Scientific Principles Medical Device Process Validation Training for Professionals Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries Overview of the New EU Medical Devices Regulations: MDR, IVDR, CE Mark and Compliance, QMS Fundamentals Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Process Validation for Drugs and Biologics QbD - Product & Process Optimization using Design of Experiments Quality Assurance/Quality Control for Biologics and Biopharmaceuticals RNA Biotechnology - An Introductory Course Technical Writing for Pharma, Biotech and Med Devices The Drug Development Process from Concept to Market 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