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UK MHRA Guidance: How to Cancel a Medicine’s Marketing Authorisation or Other Licence
In the pharmaceutical lifecycle, there are times when a marketing authorisation holder (MAH) needs to cancel a medicine’s marketing...

Sharan Murugan
Aug 192 min read
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Swissmedic Guidance: Understanding Parallel Imports and the Authorisation of Asian Medicinal Products
Switzerland’s regulatory landscape for pharmaceuticals continues to evolve, balancing patient safety with market efficiency. Two pivotal...

Sharan Murugan
May 32 min read
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UK MHRA Guidance: Apply for a Parallel Import Licence
Earlier today (05 December 2023) Medicines and Healthcare Products Regulatory Agency (MHRA) updated its guidance on Medicines: "Apply for...

Sharan Murugan
Dec 5, 20232 min read
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UK MHRA Guidance: How to get a Parallel Import Licence in UK
Earlier today Today (13 October 2022) Medicines and Healthcare products Regulatory Agency (MHRA) updated its Guidance on Medicines:...

Sharan Murugan
Oct 13, 20221 min read
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UK MHRA's: Apply for a Parallel Import Licence (Guidance Update)
Today (17 August 2022) MHRA updated its Guidance on "Medicines: apply for a parallel import licence" The guidance in general details...

Sharan Murugan
Aug 17, 20221 min read
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HPRA Guide to Parallel Imports of Human Medicines - Ireland
The Health Products Regulatory Authority (HPRA) updated its guidance on "Parallel Imports of Human Medicine" last week. Parallel...

Sharan Murugan
Apr 17, 20221 min read
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