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Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
How veterinary medicines can be advertised.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
There are changes to the legislation on reference medicinal products (RMPs) used to support abridged marketing authorisation applications.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Healthcare professionals and patients are reminded of the risk of severe asthma attacks and increased mortality associated with overuse of SABA with or without anti-inflammatory maintenance therapy in patients with asthma. Healthcare professionals should be aware of the change in...
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