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Collaboration announced at International Investment Summit, meeting the PM's ambitions to catalyse investment in the UK and proving the UK is open for business.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
This study combines a review of data on pharmaceutical firms’ CSR with interviews of representatives from 6 firms
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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