Training to various organization/academic institutes on following training modules: -
- cGMP – Basics & Principles
- WHO –GMP implementation and Documentation.
- cGMP – USFDA ( 21 CFR PART 210 & 211)
- MHRA – UK
- GMP for Medical Devices ,
- Cosmetics GMP
- Bottled water & Food GMP.
- Bulk Drug & excepients GMP
- GMP for Ayurvedic manufacturing.
- Implementation of Revised Schedule M
- Introduction to Risk Analysis & Risk Management (HACCP)
- ICH & Guidelines
- Internal Quality Audit
- Process Validations
- Analytical Method Validation.
- GMP Documentation.
- URS/FAT/SAT/DQ/IQ/OQ & PQ
- Design of Stability Studies.( ICH & WHO )
- In process Control – Integral part of GMP
- Market Recall & Market Withdrawal
- Clinical trails & Post marketing Surveillance.
- Introduction to Product Registration & Dossiers .( Regulatory Affairs)
- NEW drug development & Regulatory Market.
- Good laboratories Practices.
- Quality control & Quality Assurance.
- Hoe to start New pharmaceutical manufacturing facility.
- How to face GMP Audits.
- Pharmaceutical Packaging
- AHU – Design & Validation
- Water system : Design & Validation
- PSG- Compressed air Validations.
- Microbial validation
- Cross contamination & mix UP.
- Good ware housing practices.
- Status Labeling/ ID numbering & Colour coding
- Safety operations & Industrial safety.
- Preventive & Breakdown Maintenance.
- Cleaning & sanitation technology in Pharmaceuticals.
- Personnel Hygiene & Departmental Behaviour.
- First Aid & Health, Clothing
- Entry & Exit procedure for Man, machine & materials.
- Pest Control & Fumigations.
- Environmental Monitoring in Pharmaceuticals.
- Communication & Behavioral Training
- ISO 9000: 2000 & ISO 14001 Environmental Management Systems.
- Behavioral & Personality Development Training for Pharmacists & MR.
Especially for Students:
- How to face Interviews.
- Biotechnology & Genomics: Basics
- Pharmacy career : Scope & Challenges
- Dispensing pharmacy : India & abroad
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