Basic Good Manufacturing Practice for Quality Control Laboratory Online Course (October 27-28, 2022) – ResearchAndMarkets.com
DUBLIN–(BUSINESS WIRE)–The “Basic Good Manufacturing Practice for Quality Control Laboratory Course Online” training has been added to ResearchAndMarkets.com’s offering.
The Good Manufacturing Practice Certificate Program provides a comprehensive overview on the best practices regarding the management of manufacturing and quality control testing for pharmaceutical products.
GMP Training Overview
In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect for manufacturing high-quality products. For this reason, every staff member in the pharmaceutical industry has to be familiar with the basic GMP requirements
Learning Objectives
- You get to know the most important pharmaceutical regulations and their importance,
- you get a basic overview of GMP requirements in pharmaceutical production, and
- you become familiar with technical terms from the field of GMP and their meaning
- Understand the regulatory requirements governing GMP compliant QC Labs.
- Understand how to apply those requirements
- Understand the regulatory expectations regarding laboratory design and utilities
- Understand the regulatory expectations regarding laboratory equipment/instrumentation
Who Should Attend:
This GMP Course will be valuable to all individuals working within or managing a GMP laboratory that supports either the R&D development of a new drug product or the testing and control of commercial drug products released to the market.
Obtaining the certification would be beneficial to professionals in:
- Research and Development
- Quality Control
- Quality Assurance
- Technical Operations
- Contract Laboratories
- Regulatory affairs personnel as well as individuals who are responsible for the review or audit of such laboratory data and reports should likewise consider the value of this comprehensive certification in their positions.
Key Topics Covered:
- An Introduction to Good Manufacturing Practice (GMP),
- CFR Title 21, Parts 58, 210, 211 Overview
- GMP in the Warehouse,
- Quality Control Laboratory Design
- Microbiology in the Workplace,
- Cleaning and Sanitation,
- Good Documentation Practices – GMP Laboratory
- Documentation and Record Keeping, Stability & Training
- Contamination Control,
- Production Controls,
- Packaging Controls,
- Quality Assurance and Quality Control
- Pharmaceuticals Corrective Actions and Preventative Actions (CAPAs).
- The Regulatory Inspection
- Deviations / Non-conformances
- OOS / OOT
- How to write an effective investigation
For more information about this training visit https://www.researchandmarkets.com/r/6xjepm
Contacts
ResearchAndMarkets.com
Laura Wood, Senior Press Manager
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