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Register to vote Register by 18 June to vote in the General Election on 4 July.
Comply with good pharmacovigilance practice and prepare for an inspection.
Guidance for industry on flexible approaches we are taking on good distribution practices.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to use an ethnographic study to evaluate your digital health product.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
Your technology should adapt to future demands and work with existing technologies, processes and infrastructure in your organisation.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
How to register veterinary practice premises for veterinary surgeons to supply veterinary medicines.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Find out how to use the Trader Dress Rehearsal service to help prepare for using the Customs Declaration Service to make declarations.
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.
Compare different evaluation approaches and choose an appropriate method.
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