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Data, Freedom of Information releases and corporate reports
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Product Safety Report for Wau Wa Eczema Herbal Cream presenting a serious chemical risk.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to stop harmful weeds spreading onto land used for grazing livestock or growing crops, how to dispose of them and how to report them if they’ve spread.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Twenty packets of worming tablets seized at Border Force in Belfast.
Information about incidents and outbreaks of Ebola and Marburg, both viral haemorrhagic fevers (VHF).
AMP 5 injection for horses and dogs seized at a Belfast courier company.
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).
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
What Works to Prevent Violence against Women and Girls: funding opportunity. Aims to build knowledge on what works to prevent violence against women and girls (VAWG).
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.
How to apply for national listing of agricultural and vegetable plant varieties in Great Britain and Northern Ireland.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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.
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