Description
This cGMP Professional Certification Program is an excellent choice for gaining a strong and comprehensive understanding of GMP for pharmaceuticals. The program describes how GMP applies, globally, to the many areas of a drug manufacturing company. The program is used to train those involved in overseeing quality, auditing processes, or supervising a broad range of responsibilities within a pharmaceutical manufacturing company.
The program provides a comprehensive overview on the best practices regarding management of manufacturing and quality control testing for pharmaceutical products.
There are eleven (11) areas of focus:
- An Introduction to Good Manufacturing Practice (GMP)
- GMP in the Warehouse
- Microbiology in the Workplace
- Cleaning and Sanitation
- Documentation and Record Keeping (GDocP)
- Contamination Control
- Production Controls
- Packaging Controls
- Quality Assurance and Quality Control (QA/QC)
- Pharmaceuticals Corrective Actions and Preventative Actions (CAPAs)
- Data Integrity
Students earning this certification will have a strong understanding of industry regulations and standards. They will understand what is required to perform within federal regulations and what is necessary to maintain compliance. Students completing this program will have gained the knowledge and skills to successfully contribute within a GMP-compliant environment.
