Full form of MHRA is Medicines and Healthcare products Regulatory Agency. This agency is of United Kingdom (UK). This agency is responsible for MHRA audits throughout the world. The companies those comply their GMP regulations can export their pharmaceutical products to UK.
The GMP guidelines of MHRA are known as Orange Guide. All the GMP regulation are given in this guide that is to be followed in pharmaceutics according to MHRA guidelines.
The GMP guidelines of MHRA are known as Orange Guide. All the GMP regulation are given in this guide that is to be followed in pharmaceutics according to MHRA guidelines.
Good Manufacturing Practice Updates
- Guidance Notes for Manufacturers on Clinical Investigations to be carried out in the UK
- Inspected UK Contract GMP Quality Control Laboratories
- Blue Guide: Advertising and Promotion of Medicines in the UK
- Rules and Guidance for Pharmaceutical Manufacturers and Distributors (the “Orange Guide”)
- Good Pharmacovigilance Practice Guide
- Guideline on Process Validation
- Guide to UK GLP Regulations 1999
- Recommendations on the control and monitoring of storage and transportation temperatures of medicinal products
- A Guide to Defective Medicinal Products
- Introduction of a Risk Based Inspection Programme for GMP QC Labs
- Guidance on completion of GMP QC Lab change form - April 2009
- Inspected UK Contract GMP Quality Control Laboratories
- Other MHRA guidelines
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