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Regulatory


Amimed Direct Limited hold a portfolio of licences granted by the MHRA (Medicines and Healthcare Regulatory Agency) and the EMA (European Medicines Agency). 

We have a dedicated regulatory team within the group who have expertise within the business. 


• Maintain the full details of the Wholesale Dealer Authorisation (WDA) and Manufacturer’s/Import Licence (MIA), GMP/GDP Certificate and Home Office Controlled Drug

Licence (schedule 2-4)

• Submission of initial applications as well as Submission of renewals and any other variations

• Maintenance and updating of Standard Operating Procedures (SOPs)

• Quarterly checks of approved suppliers and company details

• Maintenance of Technical Agreements

• In house Qualified Persons (QPs)

We are in the process of implementing the Falsified Medicines Directive in compliance with the 2019 directive. 

Full GMP, MIA, TEMP control

Please click on links below to download

Amimed MIA- VER30 01-04-2019

Amimed WDA-VER5 09-01-2019

AMIMED-GDP CERTIFICATE 17168-367327-0011-03-01-2019

AMIMED-GMP CERTIFICATE 17168-367327-0010 - 12-03-2018

Home Office Licence EXP 9 MAY 2020

CD Requisition Form

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