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Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
The Defence and Security Accelerator (DASA) conducts Market Explorations to determine future activities.
Find news, information and advice from the government on starting or growing your business.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
A call for evidence launched today to explore new ways to transport captured CO2 that would enable more UK industries to adopt carbon capture technology.
How the MHRA processes variations to Marketing Authorisations (MAs)
How we work with buyers and suppliers to improve the way technology is bought across government and the public sector.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Find out if your business is eligible for tailored in-market support as part of the Export Support Service from the Department for Business and Trade.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
UKHSA Chief Executive Professor Dame Jenny Harries visits Manchester and Liverpool to launch campaign as measles cases continue to rise.
How to use a cost benefit analysis to evaluate your digital health product.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Submissions related to human medicines need to be submitted directly to the MHRA.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
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