A - Z index - R

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.

• Rachel Bosworth, Director of Communications

• Radiation dose issues in digital radiography systems

• Radiologists: Information for

• Radiology - a one-stop resource for radiology practitioners

• Radiology PACS (Picture Archiving and Communications System) - IT security

• Recalls

• Recent reclassifications

• Reclassification of medicines

• Recruitment data

• Reducing medicine risk

• Registration forms for Brokers and Active Substance manufacturers, importers and distributors

• Registration of medical devices

• Registration of medical devices: Frequently asked questions

• Regulation

• Regulation of medicines

• Regulation of Medicines Review Panel: Members

• Regulations

• Regulatory advice contact list for devices

• Regulatory guidance

• Regulatory Information Service (RIS) for medicines

• Regulatory news for devices

• Regulatory news for medicines

• Regulatory schemes that support drug development, licensing and patient access to innovative therapies

• Regulatory schemes that support drug development, licensing and patient access to innovative therapies: Regulatory initiatives

• Regulatory schemes that support drug development, licensing and patient access to innovative therapies: Scientific advice

• Rejection of submissions

• Renal medicine

• Renewal of licences

• Reporting a non-compliant Medical Device

• Reporting adverse incidents involving medical devices

• Reporting problems with herbal medicines

• Reporting safety problems

• Request for scientific advice form

• Requests for the UK to act as Reference Member State

• Requirements for submission of paediatric information required by EU Paediatric Regulation

• Research publications

• Research use only products (devices)

• Resistance of copper cables

• Responses to requests for information (RFIs) sent by the MHRA

• Responsibilities of the parties involved in the manufacture, regulation and surgical provision of vaginal meshes

• Responsibilities of the parties involved in the manufacture, regulation and surgical provision of vaginal tapes

• Retinal screening programmes: Advice on administering eye drops

• Review of EU medicines legislation ('2001 Review')

• Review of sanctions and penalties

• Review of the medicines advisory bodies structure

• Review of unlicensed medicines

• Reviews of literature

• Revision of the Clinical Trials Legislation

• Revisions to the Medical Devices and Active Implantable Medical Devices Directive

• Risk based inspections: Good Laboratory Practice

• Risk based inspections: Good Pharmacovigilance Practice

• Risk communications

• Risk minimisation, Risk Management Plans and post authorisation studies

• Risk-based inspection programme for good practice inspections

• Risk-based inspections: Good Clinical Practice (GCP)

• Risk-based inspections: Good Distribution Practice

• Risk-based inspections: Good Manufacturing Practice

• Risk-based inspections: Good Manufacturing Practice - Questions and answers

• Risks of buying herbal remedies online

• Room warning lights for dual purpose rooms

• Rosiglitazone

• RSS Feeds