GLP is the quality system applied to non-clinical safety and environmental studies during the development of new products such as medicines, industrial chemicals and pesticides. Results of GLP studies are "right." A statement that a study was conducted in conformance with GLP simply means that quality systems were followed, and that the results of the study accurately report the conduct of the study. Additionally you may be required to audit supplier companies who provide materials and/or services that are key to the work being conducted in your organisation. Developing several informational handouts on key labour rights issues, as well as a number of briefing notes on legislative instruments and policy developments. A career as a GLP QA professional will mean that you will be constantly developing your knowledge and skills. With over 60 training programs and 110 audits completed, these services empower professionals with practical skills and ensure alignment with global regulatory standards-supporting safer, research-driven pharmaceutical development and manufacturing.

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