A - Z index - M

The section presents an alphabetical listing of all pages of the website. Choose a letter from the links below to view all pages with titles that start with that letter. Alternatively view the sitemap, which lists all pages by their topic and placement in the navigation.

• MAIL: The MHRA updating service for medicines

• Making a payment to the MHRA

• Managing your clinical trial authorisation: End of trial

• Managing your clinical trial authorisation: Substantial amendments

• Manufacturer's and wholesale dealer's licences

• Manufacturers of orthoses and prostheses

• Manufacturers' Online Reporting Environment (MORE) for medical devices

• Market Surveillance and Accreditation Regulations (EC) NO 765/2008

• Marketing authorisation application forms

• Marketing Authorisation: Provisions to which it is granted

• Marketing authorisations

• Marketing authorisations: lists of granted licences

• Marketing authorisations: Types of application

• Martin Hindle

• Measles, mumps and rubella (MMR) vaccine

• Media Centre

• Medical device adverse incident reporting forms

• Medical Device Alert

• Medical Device Alerts

• Medical Device Alerts

• Medical Device Alerts

• Medical device appeals

• Medical Device Liaison Officer information

• Medical Device Technology Forum

• Medical Device Technology Forum: Forums

• Medical Device Technology Forum: Minutes

• Medical devices and medicinal products borderline

• Medical Devices Classification

• Medical Devices Directive

• Medical Devices Directive - Complying with requirements

• Medical devices: Clinical investigations

• Medical devices: Electrical safety

• Medical devices: Field Safety Notices

• Medical devices: How we monitor safety

• Medical devices: Leaving hospital with a medical device

• Medical devices: Registration

• Medical Students Elective Prize

• Medicines Act 1968 Advisory Bodies Annual Report

• Medicines Act restrictions: Exemptions from

• Medicines advisory bodies

• Medicines and your family

• Medicines Borderline Advice Form

• Medicines Commission

• Medicines Commission: Minutes

• Medicines consultations

• Medicines consultations, other

• Medicines education modules

• Medicines escalation procedure

• Medicines for children

• Medicines for children

• Medicines for children: What's new

• Medicines for Women's Health Expert Advisory Group of the Commission on Human Medicines

• Medicines Industry Liaison Group

• Medicines Industry Liaison Group: Members

• Medicines information

• Medicines learning modules FAQs

• Medicines regulation

• Medicines Regulatory Guidance

• Medicines regulatory news

• Medicines regulatory news A to Z listing

• Medicines safety monitoring

• Medicines testing

• Medicines that do not need a licence (Exemptions from licensing)

• Members

• Membership of Independent Review Panel for Advertising

• Membership of Independent Review Panel on the Classification of Borderline Products

• Membership of the Advisory Board on the Registration of Homoeopathic Products

• Membership of the Commission on Human Medicines

• Membership of the Independent Scientific Advisory Committee for MHRA database research (ISAC)

• Mercury in medical devices

• Metal-on-metal hip implants

• MHRA Divisions

• MHRA expenditure

• MHRA expenditure: Expenditure transactions over £25k

• MHRA expenditure: Five-day payment performance data

• MHRA expenditure: Government Procurement Card (GPC) transactions of £500 and above

• MHRA Portal

• MHRA speakers

• MHRA speakers: FAQs

• MHRA submission requirements for marketing authorisations, variations, renewals, PSURs and BROMI applications

• MHRA toxicology testing and collection of clinical findings upon removal of the implant

• MHRA – Medicines and Healthcare products Regulatory Agency - Home page

• MHRA/NIBSC merger

• Microbiology Advisory Committee (MAC)

• Midwives: exemptions from Medicines Act restrictions

• Ministerial Industry Strategy Group (MISG) Forum

• Ministerial Industry Strategy Group (MISG) New Technologies Advisory Panel

• Ministerial Industry Strategy Group (MISG) New Technologies Advisory Panel: Minutes

• Ministers

• Minutes of Biologicals subcommittee of Committee on Safety of Medicines

• Minutes of Chemistry, Pharmacy and Standards subcommittee of Committee on Safety of Medicines

• Minutes of Pharmacovigilance Subcommitttee of Committee on Safety of Medicines

• Minutes of the Advisory Board on the Registration of Homoeopathic Products

• Minutes of the Anti-infectives, HIV and Hepatology Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Cardiovascular, Diabetes, Renal, Respiratory and Allergy Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Chemistry, Pharmacy and Standards Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Clinical Trials Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Commission on Human Medicines

• Minutes of the Dermatology, Rheumatology, Immunology and Gastroenterology Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Herbal Medicines Advisory Committee

• Minutes of the Independent Scientific Advisory Committee for MHRA database research (ISAC)

• Minutes of the Medicines Commission

• Minutes of the Medicines for Women's Health Expert Advisory Group of the Commission on Human Medicines

• Minutes of the meetings between the Commission on Human Medicines and Industry Forum

• Minutes of the Neurology, Pain and Psychiatry Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Oncology and Haematology Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Paediatric Medicines Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Patient Information Expert Advisory Group of the Commission on Human Medicines

• Minutes of the Pharmacovigilance Expert Advisory Group of the Commission on Human Medicines

• Mixing medicines in palliative care

• MLXs: Medicines consultation letters

• MMR Vaccine

• Mobile communications interference

• Mobile phones

• Mobile phones in hospitals: Frequently asked questions

• Model Publication Scheme

• Monthly lists of letters for healthcare professionals on the safety of medicines

• MORE: Manufacturers' Online Reporting Environment for medical devices

• Mutual Recognition Agreements

• My medicine: From laboratory to pharmacy shelf