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Find out about partial exemption and the methods and calculations to use to see how much input tax you can recover.
How to approach sampling ambient air and the sampling and analytical techniques to use.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Find out about gaining approval for a fair partial exemption special method if you deal with partial exemption for insurers.
Find out about partial exemption special methods for government departments.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
What best available techniques are, when you must follow them, how to propose alternatives and how to refer to them in your application.
Guidance for Applicants wishing to apply for a Promising Innovative Medicines designation, pre-submission meeting or an EAMS Scientific Opinion.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
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