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Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
The AQuA Book is Government guidance about how to produce robust, fit for purpose analysis. It's for all analysts, analytical managers and commissioners.
The Foreign, Commonwealth & Development Office is committed to providing a high-quality service to everyone we deal with.
How to use a cost utility analysis to evaluate your digital health product.
UK guideline on GMP for decentralised manufacturing, ensuring compliance with EU GMP principles for safe, quality medicinal products.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
How to use a before-and-after study to evaluate your digital health product.
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