(CCCP) Clinical Compliance Certified Professional

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. 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.

Certification Program FAQs:

Certification Requirements:

  1. Choose 3 Core Courses from any of the courses listed below.
  2. Choose 1 Elective Course from any of our other classroom courses.
Skill Level
Course Name
Advanced Advanced Topics for Biostatistics for Non-Statisticians
Foundational Advanced Blockchain Concepts for the Pharmaceutical and Medical Device Industries
Foundational Adverse Drug Events – Understanding and Reporting Requirements
Foundational Biostatistics for Non-Statisticians
Advanced Clinical Trial Design For Medical Devices
Advanced Clinical Trial Project Management, Phase 1-4 Best Practices
Advanced Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
Foundational GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials 
Foundational Good Clinical Practices (GCP) & Risk Based Monitoring- Understanding and Implementing Current Global Requirements 
Advanced Integration of Risk Management Principles and Activities into the Quality System
Foundational Introduction to Molecular Biology Techniques – Applications in the Biotechnology and Pharmaceutical Industries
Foundational Introduction to Statistical Analysis of Laboratory Data
Foundational Pharmaceutical Production Batch Record Review
Foundational Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy
Qualifying, Management and Auditing of Contract Manufacturing Organizations
Foundational QbD - Product and Process Optimization using Design of Experiments
Advanced Selecting and Managing CROs
Foundational The Drug Development Process from Concept to Market
Advanced Understanding & Implementing New EU Clinical Trial Regulation & GDPR

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

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