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How to prepare for implementation and compliance of the Safety Features Regulation.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Guidance for prescribing vets on the use of the cascade.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
You must get permission to export certain drugs and medicines.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
Advice for healthcare professionals on the reclassification of codeine linctus to a prescription-only medicine (POM), following a public consultation.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
It's illegal to drive if you're unfit to do so because you're on legal or illegal drugs, or you have certain levels of drugs or medicine in your blood
How UK citizens or residents can get healthcare when visiting countries or territories outside the EU where the UK has reciprocal healthcare agreements.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Anyone in Northern Ireland selling medicines to the public via a website must still comply with the requirement to apply the EU common logo.
People are urged to seek advice from healthcare professionals if they feel they have become dependent on or addicted to codeine linctus.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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