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Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
You can make observations on the patentability of a published patent application.
This guide provides information about being arrested in Germany and what conditions are like in prison there.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to spot Aujeszky’s disease, what to do if you suspect it and measures to prevent its spread.
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Form A64A: Application to receive information from court records about a parental order.
Find details of recent trade mark applications or amendments by searching the journal
Information from the National Health Service on conditions, treatments, local services and healthy living
Explainer for the pharmaceutical industry on Pharmacovigilance requirements mitigations to bridge the gap between the implementation of the EU Regulation on veterinary medicines and the revised Veterinary Medicines Regulations as they have an effect in Great Britain (GB VMR).
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Find out about local procedures, burials and cremations, and returning the body to the UK.
Guidance and regulatory advice on how to apply for licences issued under ASPA and how your compliance with ASPA and your licence conditions will be assessed.
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