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How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Advice on writing clear notices and maximising replies to your FSNs.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Apply for a higher education course, track your application and accept or reject your offers.
Details of General Licences issued by OFSI
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
List of fees for consular information in the USA.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Make sure that domains that do not send email cannot be used for spoofing.
Get information on teacher training courses, funding, pay scales and how to make a great application
Pharmacovigilance system requirements
Form to report patients meeting the case definition.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
This document explains: how patients are tested and treated, and steps in place to prevent its spread.
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