GMPs are set practices that makers need to set up to guarantee that their items meet indicated quality norms.
GMP rules comprise of the base prerequisites that sustenance item, medication or pharmaceutical makers need to meet to guarantee that their items are of the recommended quality and make no mischief or hazard the individuals who devour them or people in general on the loose.
Here are 10 basic GMP best practice guidelines to follow:
- Establish Good Written Procedures
- Qualify and Validate Processes
- Identify Roles and Responsibilities
- Keep All Records
- Use the Right Facilities and Equipment
- Assemble a Competent Team
- Practice Good Hygiene
- Maintain Facilities and Equipment
- Ensure Quality
- Use GMP Audit Checklists
Good manufacturing practices, or in short GMP, are the practices required to comply with the guidelines, issued by international inspection organisations such as FDA, MHRA, EMA, and other. These guidelines are the minimum requirements that pharmaceutical or food product manufacturers need to follow to guarantee the high quality of the products that they manufacture. If these guidelines are not followed properly, the developed products may pose serious risk to people’s health – there may be risk of cross-contamination, infections or other. In order to achieve best results and strict control, organizations apply these good practices to the whole personnel that is involved in the development process of drugs, food and other.
A great source of information about GMP are books like ‘’Good Manufacturing Practices for Pharmaceuticals’’; ‘’ Good Manufacturing Practices for Pharmaceuticals: A plan for total quality control from manufacturer to consumer; ‘’ Good Manufacturing Practices for Pharmaceuticals: A plan for total quality control’’ and many others.