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Understanding Contract QP, RP & RPi Services: What You Need to Know
Navigating the pharmaceutical industry’s complex regulatory framework requires expert guidance, especially in roles like Qualified Person (Q
Ghanshyam Kanani
Nov 20, 20242 min read
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Setting Up a WDA License and Wholesale Licenses in the UK
Learn how to set up a WDA license for UK pharmaceutical distribution, covering MHRA steps, compliance, and sector-specific requirements
Ghanshyam Kanani
Nov 13, 20243 min read
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How to Set Up MHRA & EU Licenses for Your Pharmaceutical Business
Setting up a pharmaceutical business in the UK or EU requires stringent regulatory compliance.
Ghanshyam Kanani
Nov 11, 20245 min read
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A Comprehensive Guide to Importing Medicines from Approved Countries for the UK Market
As the regulatory landscape continues to evolve post-Brexit, importing medicines into Great Britain from European Economic Area (EEA)...
Ghanshyam Kanani
Sep 17, 20244 min read
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Implementation of Labelling and Packaging Requirements for Medicinal Products Under the Windsor Framework: Key Guidelines
Following the regulatory changes post-Brexit, the implementation of the Windsor Framework aims to enhance the efficiency of the supply...
Ghanshyam Kanani
Sep 17, 20243 min read
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Understanding Recent Changes in MHRA Guidelines for Good Distribution Practice (GDP)
The Medicines and Healthcare products Regulatory Agency (MHRA) plays a pivotal role in ensuring the safety and quality of medicinal...
Ghanshyam Kanani
Apr 22, 20243 min read
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