MHRA - Selecting the right subject area

Speaker request form help

Select ’Chief Executive or Chairman’ if you would like the Chief Executive or Chairman to speak at your event.

Select ’Device Technology & Safety’ if you want a speaker to talk on:

Select ’Information about and communicating with the MHRA’ if you want a speaker to talk on:

’MHRA in an hour’ - An introduction for those who are not familiar with our work
How the MHRA communicates with its stakeholders
Careers for scientists, phamacists and doctors at the MHRA

Select ’Information Management’ if you want a speaker to talk on:

Select ’Inspection, enforcement and standards’ if you want a speaker to talk on:

Select ’Licensing of medicines’ if you want a speaker to talk on:

Drug Development and Clinical Trials
New active substances/medicinal products/routes of administration and formulations
Advice on product licence applications, including generic and parallel imports
Registration of herbal or Homeopathic Products
Advanced therapy medicinal products
The role of MHRA in Marketing authorisations and licensing
Variations to product licences
National and European licensing

Select ’Monitoring of medicines on the market’ if you want a speaker to talk on:

Pharmacovigilance
E2B, electronic reporting of adverse drug reactions to medicines
Yellow Card Scheme - reporting adverse drug reactions
renewal of marketing authorisations
reclassification of medicines
Product and patient information, including Braille and user testing requirements
Advertising and promotion of medicines
Pharmacovigilance Risk Management and Pharmacovigilance Signal Management
Therapeutic Reviews of medicines
Information for Public Health
Special populations and Paediatric Regulations

Select ’Policy relating to medicines and medical devices’ if you want a speaker to talk on:

Traditional Herbal Medicinal Products Directive, Herbal medicines regulation and safety
Prescribing & Better Regulation Policy
Herbal Medicines & New Technologies Policy
Strategy & European Medicines Policy
International & Parliamentary affairs
Devices Policy, European & Regulatory Affairs
Registration and classification of medical devices
Clinical investigations for medical devices
Enforcement of the European directives on medical devices

Select ’Safe use of medical devices’ if you want a speaker to talk on:

select ’Not sure/don’t know’ if you do not know what subject area your event/presentation falls into.