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Nowadays all regulatory authorities focus on data integrity and have their own data integrity guidelines - however, their regulations don’t always agree. With this e-book you will understand all the requirements! This report details the ins and outs of all three documents of EMA, MHRA and WHO and explains how the FDA regulations fit in.
e-book
111 pages
ISBN: 978-3-958070912
1st edition 2018
Delivery immediately after receipt of payment
€345.00 net
Excerpt from the GMP Compliance Adviser Nowadays all regulatory authorities focus on data integrity. The European Medicines Agency (EMA) — the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) — and the World Health Organization (WHO) — all have data integrity guidelines. And, their regulations don’t always agree. You’ll understand all the requirements with Data Integrity in the EU: Requirements for Quality Management Systems. This report details the ins and outs of all three documents and explains how the FDA regulations fit in. You will learn:
The report also includes the texts for:
Order your copy of Data Integrity in the EU and avoid data problems and breaches that can damage your drug’s success.
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