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Register to vote Register by 18 June to vote in the General Election on 4 July.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How to set up a public service mutual and 'spin out' of a public service organisation.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Submission dates and how the submissions using the EC decision reliance procedure work.
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.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
How the MHRA processes variations to Marketing Authorisations (MAs)
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.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
The seeds which must be certified before you can market them, how to get them certified and how to get a licence for your seed business.
How to renew marketing authorisations for products granted through different routes and at different times.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
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