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Date	Title
07/06/2013	Guide to Interchangeable Medicines
21/05/2013	Guide to electronic submissions - human medicines
09/05/2013	Guide to Fees and Fee Application Form for Human Products 2013
13/03/2013	Guide to Electronic Transmission of ICSRs and SUSARs associated with the use of Human Medicines
06/03/2013	Guide to refusals and appeals
05/03/2013	Guide to Parallel Imports - Human Medicines
28/02/2013	Guide to hospital-based advanced therapy medicinal products
27/02/2013	Application for a variation to a manufacturing/importation authorisation or wholesaler's authorisation
14/02/2013	Registration for active substance manufacturers, importers and distributors
15/01/2013	Clinical Trial Subcommittee Meeting Dates and Application Cut-off Dates for 2013
14/01/2013	Guide to Clinical Trial Applications
21/12/2012	Registration for brokers of finished medicinal products
30/10/2012	Guide to reporting of quality defects
14/08/2012	Guide to Notification of Marketing Status of Human Medicines
22/05/2012	Guide to labels and leaflets of human medicines
11/05/2012	Guide to submission of Risk Minimisation Plans
10/04/2012	Guide to Invented Names of Human Medicines
12/03/2012	Guide for suppliers of first aid kits, containing medicinal products, supplying solely to the end-user
17/11/2011	Guide to Transfers of Product Authorisations and Parallel Product Authorisations for Human Medicines
07/11/2011	Guide to PharmaTrust extranet