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Submissions related to human medicines need to be submitted directly to the MHRA.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
Pharmacovigilance system requirements
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Forms to make a variation to a Blood establishment Authorisation
The Lambert toolkit is for universities and companies that wish to undertake collaborative research projects with each other.
The laws on selling, buying and carrying a knife or weapon depend on the type of knife or weapon, your age and your circumstances.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Information about new applications, post-licensing, advertising, product information and fees.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Providing vital research into COVID-19 immunity and vaccine effectiveness nationally.
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