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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Check if you need a visa or permit to work in Portugal and how to get one if you do.
Information for manufacturers.
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
We are a specialist list set up to deal with: claims and appeals concerning patents (including supplementary protection certificates), registered designs, copyright issues, trade marks, semiconductor topography rights and plant varieties; claims and appeals concerning the and other intellectual property...
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Information from the National Health Service on conditions, treatments, local services and healthy living
You need a certificate to export rough diamonds.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
Find out details of the Procedure Codes and Additional Procedure Codes (both Union and National) excluded from use with Simplified Declaration Procedure (SDP) with regular use and Entry in Declarants Records (EIDR).
Sign up for alerts about applications for UK trade marks or international registrations
Check what side effects people have reported when they've taken a medicine.
This guidance describes case definitions to inform testing and reporting of suspected mpox cases.
Certification Officer (CO) decisions made in response to complaints and applications.
GPC data for Government Legal Department, Attorney General’s Office and HM Crown Prosecution Service Inspectorate, monthly from 2015.
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