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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


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


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
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
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


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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