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Steps for assuring quality under extreme time constraints
The framework provides the MOD and industry partners with the necessary understanding of government quality assurance .
Guidance for business and government departments.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
This document explains the Down’s syndrome screening quality assurance support service (DQASS) and how to use it.
Certification for good quality combined heat and power (CHP).
How to use a cost utility analysis to evaluate your digital health product.
Proficiency testing (PT), also known as external quality assessment (EQA), allows the introduction of samples of known but undisclosed content into a laboratory’s routine testing procedure.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Routine quality control test procedures for full field digital mammography (FFDM) systems in NHS breast screening programmes.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Legal aid providers: find out how the LAA sets quality assurance standards and make sure you qualify.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
This document provides information on internal quality control and assurance procedures, and external quality assessment.
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