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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 how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Using an ecological momentary assessment to evaluate your digital health product.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
All marketing and advertising must be: an accurate description of the…
Advertising to consumers The Consumer Protection from Unfair Trading…
There are 2 advertising codes of practice that describe how businesses…
You must describe your product accurately. This means if you make a claim…
You must check if customers want to be contacted by fax, phone, post or…
How to use a behaviour change techniques review to evaluate your digital health product.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Southern Region, Judge E Morrison on 1 June 2021
Working with others to embed the importance of place within the published guidance.
Requirements for Immunological Veterinary Medicinal Products.
How to use a quasi-experimental study to evaluate your digital health product.
Find out how to contact HMRC to help you get a commodity code and what information you’ll need to send us.
MCA interpretation of the certification and vehicle/container packing certificate requirements of the International Maritime Dangerous Goods (IMDG) Code.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a cost utility analysis to evaluate your digital health product.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Technical advice and guidance for licence holders.
Explains what local authorities should do before publishing their data.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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