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Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Information for manufacturers.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Keep up to date with the latest information from the UK GLP monitoring authority.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Export controls on goods that can be used for torture or capital punishment.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Check if you can operate a facility and meet the conditions to store imported goods temporarily and find out how to apply.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
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