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Decision on application for authorisation under UK REACH.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Volume 42 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
The CMA is investigating Microsoft Corporation’s (Microsoft) hiring of certain former employees of Inflection AI, Inc. (Inflection AI) and its entry into associated arrangements with Inflection AI.
Volume 33 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 38 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Inspection plans for the Independent Chief Inspector of Borders and Immigration (ICIBI).
Volume 53 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Information on how to use a High Integrity Telecommunications System.
Volume 22 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Management information on the number and outcomes of online education accreditation scheme (OEAS) quality assurance commissions carried out by Ofsted.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Volume 50 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
PPC Applications and Decisions for Large Combustion Installations 2024
Volume 10 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This series brings together all documents relating to TAB terms or reference
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