(CCCP) Clinical Compliance Certified Professional™

View Required Courses Certification FAQs

About the Clinical Compliance Certification Program

The Clinical Compliance Certified Professional (CCCP) program is ideal for individuals involved in the clinical stages of drug development and are interested in regulatory compliance certification. The CCCP 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

This regulatory compliance program curriculum is designed to give participants a thorough, practical understanding of all clinical phases from both a regulatory and procedural perspective.

Clinical compliance training attendees will gain comprehensive insight into early drug development, the role of the FDA and other regulatory bodies and the requirements of trial monitoring and reporting adverse events - pre and post approval.

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)

Advanced Topics in Biostatistics for Non-Statisticians Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Auditing and Qualifying Suppliers and Vendors Biostatistics for Non-Statisticians Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Clinical Document Management: A Trial-by-Trial Compliance Approach Clinical Trial Project Management, Phase 1-4 Best Practices Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products 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 European Regulatory Procedures - EMA & National Requirements FDA Inspections - What Regulators Expect and How to Prepare

GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials GMP Training for the QC Laboratory Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements Integration of Risk Management Principles and Activities into the Pharmaceutical Quality System Introduction to Statistical Analysis of Laboratory Data Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries Oncology Drug Development Course - A Comprehensive Overview Pharmaceutical Production Batch Record Review Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy QbD - Product and 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 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

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