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How you import from and export to Turkey.
Information for PO's on how to gain recognition, produce annual reports, submit production and marketing plans and ensure compliance.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How to ensure the products you make or import comply with the law and are safe for consumers to use.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
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