Training

For more information on quality and regulatory training, please contact Global Regulatory Inc. at 403-770-1994 or email us

International Regulatory Training

In-house, off-site or on-line quality and regulatory training programs, webinars, workshops, courses, programs, continuing education, and seminars such as

International Regulatory Education and Training
- US Food and Drug Administration (FDA)

Good Manufacturing Practices (GMP)
Good Laboratory Practices (GLP)
Good Clinical Practices (GCP)
Quality System Regulations (QSR)
Food, Drug & Cosmetic Act (FD&C)
NELA Nutritional Labeling
CFR Part 11
Japanese Ministry of Health, Labor, and Welfare (MHLW)Pharmaceutical Affairs Law (PAL) of 2002
Health Canada
CMDCAS
Australia Therapeutic Goods Agency (TGA)
Therapeutic Goods Act 1989
Australian Regulatory Guidelines for Complementary Medicines (ARGCM)
Therapeutic Goods (Medical Devices) Regulations 2002
Brazil INMETRO
European Union CE Marking
EEC Directives
CEN Standard

Quality Systems Education and Training
- Quality Manual Development
- Quality Standard Operating Procedures
- Failure Investigations
- Quality Control
- ISO
- CAPA Systems
Manufacturing, Processing, and Production Education and Training
- Bioprocessing
- Lyophilization
- Fermentation
- Aseptic Processing
- Filtration
- Sterilization
- Packaging
- Filling
- Storage and Handling
Technical Education and Training
- Qualification and Validation
- Software Validation
- Design Controls
- Mathematics and Statistical Controls
Facilities Education and Training
- Plant Design and Construction
- Water Systems
- HVAC Systems
- Air Systems
- Occupational Health
- Safety
Scientific Education and Training
- Microbiology
- Chemistry
- Pharmacology
- Pharmacokinetics
- Toxicology

For more information, please contact Global Regulatory Inc. at 403-770-1994, email us or Submit Regulatory Requests for Proposals

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Training

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