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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
Sir Martyn Oliver spoke about the Big Listen, the changes Ofsted is making and taking the time to collaboratively build a better education system for all.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Comply with good pharmacovigilance practice and prepare for an inspection.
Surveys of English farming practices.
Using an ecological momentary assessment to evaluate your digital health product.
Actions that trial sponsors should consider to build resilience into clinical trial design
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to use an ethnographic study to evaluate your digital health product.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
To help you protect, manage and enforce your intellectual property (IP) rights in Philippines.
The Company Names Tribunal practice direction provides the framework for the management of proceedings brought before the Tribunal.
Practice notices announce changes to our practice, such as how we interpret a provision of the law, or how we handle applications.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use a randomised controlled trial to evaluate your digital health product.
Codes of practice and conduct for forensic science providers and practitioners in the criminal justice system.
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