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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…
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Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Steps SMEs can take when bidding for government contracts so they can compete with larger companies.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Submission dates and how the submissions using the EC decision reliance procedure work.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to use a cost effectiveness analysis to evaluate your digital health product.
How to request and manage school-led initial teacher training (ITT) places for School Direct.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How the MHRA processes variations to Marketing Authorisations (MAs)
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
The effectiveness of marketing channel liberalization in increasing competition among traders and prices obtained by farmers for their produce
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.
Examples of successful initial teacher training (ITT) marketing campaigns.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
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