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A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Find out how to account for VAT schemes on business gifts, samples and promotional schemes.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Once your business is established and you’re making a profit on the…
Growing your business, whether through increased sales or improved…
How you go about increasing sales depends on your circumstances and how…
One way of finding new customers for your products and services is by…
If you’re looking to grow your business by improving your products and…
If you’re planning to develop new products and services, you should test…
As your business expands, you’ll need more capacity to produce or provide…
Business mentors can help you develop your ideas for growth by sharing…
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
We advance prosperity by ensuring no viable UK export fails for lack of finance or insurance, doing that sustainably and at no net cost to the taxpayer.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Organisational definitions of terms concerned with risk and risk-related matters.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
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