MHRA Guidelines : Pharmaguideline

Online GMP Courses with Certificate

ENROLL

MHRA Guidelines

Regulatory guidelines by Medicines and Healthcare products Regulatory Agency- UK MHRA including GMP - Orange Guide, Validation, GLP etc.in pdf format.
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.

Good Manufacturing Practice Updates






Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of pharmaguideline.com, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips.
.moc.enilediugamrahp@ofni :liamENeed Help: Ask Question


1 comment: Post Yours! Read Comment Policy ▼

  1. Difference between USFDA and MHRA gaidline for finished product

    ReplyDelete

Please don't spam. Comments having links would not be published.


Popular Categories

QA SOPs QC SOPs Micro SOPs HVAC Production SOPs Stores SOPs Checklists Maintenance SOPs HPLC Sterile GLP Validation Protocols Water System GDP Regulatory Maintenance Calibration Warning Letters Education B.Pharmacy
Online Courses


Follow Pharmaguideline


DOCUMENTS

PHARMACEUTICAL DOCUMENTS




Editable Pharmaceutical Documents in MS-Word Format. Ready to use SOPs, Protocols, Master Plans, Manuals and more...

View


adsbypg


Recent Posts