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Register to vote Register by 18 June to vote in the General Election on 4 July.
American viticultural area
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
The British Consulate General in Boston maintains and develops relations between the UK and the USA.
Upper Tribunal Administrative Appeals Chamber decision by Judge Wikeley on 08 May 2024
Find out where SPZs are, what defines the different zones and why the Environment Agency must protect groundwater from pollution.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
What private maritime security companies (PMSCs) with a trade control licence must do when their circumstances change like leaving the sector or merging.
How to renew marketing authorisations for products granted through different routes and at different times.
Submissions related to human medicines need to be submitted directly to the MHRA.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Information about jobs in Massachusetts supported by UK companies, and Massachusettsan exports to the UK.
Free and impartial help with money and pensions.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
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.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How to manage the burial of animal remains to prevent or limit groundwater pollution.
How the MHRA processes variations to Marketing Authorisations (MAs)
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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