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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Form for a business to register seed marketing operations.
UKHSA Chief Executive Professor Dame Jenny Harries visits Manchester and Liverpool to launch campaign as measles cases continue to rise.
Find out the rules from 1 January 2018 if you promote or use arrangements that are meant to give someone a VAT or other indirect tax saving or a tax deferral.
Information for entertainers and musicians, from non-visa national countries, such as EU Member States and the US, visiting the UK for performance and work.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Understand and avoid all types of anti-competitive and cartel activity including price-fixing, collusion, bid-ridding and sharing markets. Know how to report concerns to the CMA.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
This page provides a guide for those interested in key upcoming digital regulatory activity being explored, developed or implemented by government. It covers a range of governance activities, from legislative change to the development of co-regulatory and self-regulatory frameworks.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
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