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Certification Categories:
- GMP: Good Manufacturing Practice
- GMP Auditing: FDA Inspection Readiness
- GLP: Good Laboratory Practice
- GCP: ICH Good Clinical Practice
- GDocP: Data Integrity & Documentation
- GPP: Good Pharmacoepidemiology Practice
- GVP: Good Pharmacovigilance Practice
- GDP: Good Distribution Practice
- Quality Assurance (QA) – Pharma & Device
- QRM: Quality Risk Management
- Drug Safety & Pharmacovigilance
- Regulatory Affairs (Pharma & Device)
- Validation: Process & Equipment
- CSV: Computer System Validation
- CSA: Computer Software Assurance
- OSHA / HR EEO for Employees
- Change Control Training
- Equipment Qualification & Commissioning
- FDA 21 CFR Part 211: GMP Drug Mfg.
- FDA 21 CFR Part 117: GMP Food Mfg.
- FDA 21 CFR Part 820: GMP Device Mfg.
- FDA 21 CFR Part 11: Electronic Records
- EU MDR: Medical Device Regulation
- MDSAP: Device Single Audit Program
- ISO 14971:2019 – Medical Devices
- ISO 13485:2016 – Medical Devices
- ISO 14155:2020 – Medical Devices
- GMP: Refresher Training
- GMP: For Beginners
- Clinical Research Training Programs
- CRA: Clinical Research Associate
- CRC: Clinical Research Coordinator
- Clinical Trial Training: Sponsors & CROs
- HIPAA & GDRP in Clincal Research
- Pharmaceutical Microbiology
- Contamination Control & Aseptic Techniques
- Pharmaceutical Sales & Marketing