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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance on promoting healthy and safe communities.
How to apply for marketing authorisation via this new procedure.
Business plans - download free templates and get help writing a business plan
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
This review provides a cross-country comparison of trade promotion organisations to identify countries of interest for an in-depth follow-up study.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Submissions related to human medicines need to be submitted directly to the MHRA.
How the MHRA processes variations to Marketing Authorisations (MAs)
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance to renew your marketing authorisation including the renewal form.
Resources to help local commissioners achieve value for money by estimating the return on investment (ROI) and cost-effectiveness of public health programmes.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to find out information on our social impact activities and programmes.
Detailed guidance on advertising and promoting medicines.
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