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This guide provides an overview of the inspection data summary report (IDSR) for primary and secondary schools, including schools with a sixth form and gives guidance on interpreting the data.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
Information about the EU Regulations and their implementation in Northern Ireland
An overview of the changes made to the Railways (Interoperability) Regulations 2011 that came into force on 1 January 2021.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
How to use a quasi-experimental study to evaluate your digital health product.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Guidance primarily aimed at local responders covering some common issues that may arise during the Recovery Phase of an emergency in the UK.
How to apply for marketing authorisation via this new procedure.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Disclosure of the identity of individuals making applications and complaints to the Certification Officer
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
Don’t include personal or financial information like your National Insurance number or credit card details.
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