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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Employers' responsibilities when using agencies to find staff, including health and safety, access to facilities, vacancies, continuous employment, transfer fees and complaints
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
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.
How to apply for marketing authorisation via this new procedure.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Find out if you’re a trust or company service provider who needs to register for supervision with HMRC under the money laundering regulations.
Submissions related to human medicines need to be submitted directly to the MHRA.
HESA collect, process and publish data about higher education in the UK, supporting and enhancing the competitive strength of the sector. HESA works with the Department for Business, Innovation & Skills .
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
Pharmacovigilance system requirements
Find out how the Rural Payments Agency (RPA) handles your personal data
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.
British Educational Communications and Technology Agency, was a non-departmental public body and lead agency in the United Kingdom for promotion and integration of information and communications technology (ICT) in education.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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