Good Laboratory Practices (GLP) Certified Compliance Professional™ (GLPCP)

View Required Courses Certification FAQs

About the Good Laboratory Practice Certification Program

The Good Laboratory Practices Certification for Compliance Professionals (GLPCP) program is a comprehensive certification and training program covering GLP training. The GLPCP 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.

CfPIE’s GLPCP is intended for those who work in a GLP regulated-environment and are responsible for compliance. Subjects in this good laboratory practices training range from pre-clinical in-lab requirements through post-approval and manufacturing concerns.

Since a solid GLP certification compliance program can have such a significant impact on efficient, cost-effective drug development and production, personnel with a qualified understanding of these regulations are always in high demand.

Also see: GLP Facility Certification Program

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 Advanced Topics in Biostatistics for Non-Statisticians Analytical Chemistry Principles for Pharmaceutical Scientists Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic 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 Computer System Validation Development and Validation of Bioanalytical Assays for Biologics: Quantitation (PK) and Immunogenicity Assays Effective Document Management for Pharma, Biotech & Medical Device Ethics in Research - Values for Responsible Conduct of Research

FDA Inspections - What Regulators Expect and How to Prepare Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Human Error Prevention (HEP) - Risk Factors and Strategies Integration of Risk Management Principles and Activities into the Pharmaceutical Quality System Introduction to Statistical Analysis of Laboratory Data Introduction to Vaccines - CMC Regulatory and Quality Aspects Laboratory Equipment Validation and Qualification Oncology Drug Development Course - A Comprehensive Overview Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Process Validation for Drugs and Biologics 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

Since 2006 CfPIE has