Dry Granulation Training for the Pharmaceutical Industry

On completion of this course, learners will be able to understand the complete manufacturing process for pharmaceutical dry granules. They will master the critical stages of dry granulation: blending, compaction and milling. They will identify the applicable quality and safety standards (BPF, GMP) and apply good practice to guarantee compliance with regulatory requirements.
Finally, they will be able to use the appropriate production equipment and technologies.

TRAINING PROGRAMME
> Introduction to dry granulation: Definition and principles / Advantages over wet granulation
> Stages of the manufacturing process: Powder blending / Compaction (roller compaction) / Milling and sizing
> Standards and regulations: Good Manufacturing Practice (GMP) / Regulatory authority requirements (EMA, FDA)
> Quality and safety management: Control of critical points (CCP) / In-process control (IPC)
> Practical work: Use of granulation equipment / Monitoring of production parameters (pressure, granule size)
> Skills assessment: Multiple-choice test at the end of the course / Simulated workplace scenario

Target audience:
Pharmaceutical production operators, Manufacturing technicians and engineers, Quality and production managers

Experience level:
Basic knowledge of pharmaceutical manufacturing processes.

Duration:
2-day session (14 hours, adaptable for customised modules)

Accessibility for people with disabilities:
Please contact us if you require disability accommodations