- Overview
- Agenda
- Features
- Justify This Training
- FAQ
Watch Trailer
Agenda
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Understanding cGMP
Details the role, rationale, and importance of global current good manufacturing practices (cGMP) for drugs, medical devices, and blood.
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cGMP Pillars 1-3
Explains the roles and rationale of cGMP compliance, covering quality management systems (QMS), premises and equipment, and personnel training.
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cGMP Pillars 4-6
Explores the roles and rationale of cGMP compliance, covering materials management, documentation and records, and validation and qualification.
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cGMP Non-Compliance
Outlines how regulatory audits, establishment inspection reports (EIRs), and 483 remediations shape risk and reputation.
Features
- Closed Captioning in English, Spanish, French, French Canadian, Hindi, Japanese, Korean, Mandarin, Russian, Standard Arabic
- Transcripts in English, Spanish, French, French Canadian, Hindi, Japanese, Korean, Mandarin, Russian, Standard Arabic
- Course materials
- Real-time tracking
- Progress reporting
- Accessibility features
- Corporate account upgrades
- LinkedIn certificate attachment
- Verified certificates
Justify This Training
View our “Justify This Training” checklist and letter to craft a persuasive request that clearly shows the value of Biotech Primer training to your role and your company. This step-by-step guide helps you highlight ROI, align with business goals, and increase your chances of getting this course approved.
FAQ
Our Executive
Certifications
Cannot make our live class? Consider one of our Executive Certifications.

Drug Development Executive Certification
- CPE:13.50 Credits
- Time:10.5 Hours
- Total:12 Courses

Drug Manufacturing Executive Certification
- CPE:14.50 Credits
- Time:10 Hours
- Total:11 Courses


