GMP GUIDE | GMP CQV Pharma Training | GMP for FREE
Welcome to the GMP GUIDE. Your ultimate GMP GUIDE for the pharmaceutical industry, CQV, project management, and lab excellence!
Located in Switzerland 🇨🇭 (Leader in Pharma industry) and with over 25 years of professional GMP experience.
We dive deep into high-demand GMP topics like quality management, CAPA (Corrective and Preventive Actions), GMP guidelines, validation, qualification, SOPs (Standard Operating Procedures), AI, Compliance and quality assurance principles.
Target Audience for GMP Training:
* Emerging professionals and students in pharmacy, chemistry, and other life sciences.
* Quality Assurance (QA) and Quality Control (QC) personnel, including team members and managers.
* Validation and qualification specialists CQV involved in equipment and process verification.
* Educators and trainers who teach GMP principles and practices.
* Manufacturing and production staff, including supervisors, managers, and operators.
* Auditors and inspectors conducting GMP inspections.
Aseptic Valves in Pharmaceutical Industry | Free GMP CQV Training Course 2025
Pest Control in Pharmaceutical Industry | Free GMP CQV Training Course 2025
Welding in Pharmaceutical Industry | Free GMP CQV Training Course 2025
Stainless Steel 316L in Pharmaceutical Industry | Free GMP CQV Training Course 2025
Calibration | Free GMP CQV Training Course 2025
Airlocks in pharmaceutical manufacturing | Free GMP CQV Training Course 2025
Quality by Design QbD
Pharmaceutical Recalls, Causes, and Quality Compliance
Avoiding FDA pitfalls
Pharmacopeial Analytical Method Verification and Validation
202 FDA NDA and BLA Response letters and how to solve them
Capsule Filling Machine Qualification | How to qualify a Capsule Filling Machine?
Dry Powder Mixer Qualification | How to qualify a Dry Powder Mixer?
Fluid Bed Dryer Qualification | How to qualify a Fluid Bed Dryer?
Tray Dryer Qualification | How to qualify a tray dryer?
Tablet Manufacturing Process Explained
Autoclave Operation, Safety, and Validation
Annex 22 GMP | Alcoa Data Intergity and the future of Pharma with AI
Change Control in Pharmaceutical Industry | Good Manufacturing Practice
HACCP vs HARPC
Cleanroom qualification | How to perform clean room qualification
Computer Software Assurance CSA | The future of Computer System Validation CSV | CSV CSA Training
What is Qualification and Validation | GMP Annex 15 explained in 2 minutes! Pharma GMP Training
What is Batch Record Review? Explained in 2 minutes! | Free GMP Training video 2025
GMP Annex 1 explained in 2 minutes! | Good Documentation Practice | Free GMP Training video 2025
Ask any Pharma Question | Explaining Good Manufacturing Practices for free
Quality Assurance | Free GMP CQV Training Course 2025
The Qualified Person QP | Free GMP CQV Training Course 2025
Clean Steam Generator Qualification | Free GMP CQV Training Course 2025
Good Manufacturing Practice | QMS Personnel Equipment Good Documentation Practice | GMP Training