Since 2016, the Acorn Regulatory publications on issues such as pharmacovigilance, medical device regulations, Brexit and more. Each of the whitepapers offers readers the opportunity to read insights from some of the expert team at Acorn Regulatory. Our team works hard to produce compelling whitepapers and articles each month and you can download any of the whitepapers here. Here are just some of the whitepapers that are available right now:
Our second Acorn Regulatory MDR whitepaper looks at the issues of unique device identifiers, the role of Eudamed under MDR and post-market surveillance.
The Acorn Regulatory medical devices team has looked at the major issues that will impact on device manufacturers and suppliers. Download it here.
Our expert eCTD publishing team has written several whitepapers on issues relating to electronic publishing. Now, they have compiled the most popular articles from recent months into a free whitepaper for you to download. Download the eCTD whitepaper here.
‘Selected Writing from Acorn Regulatory’ highlights just some of the most read articles written by our expert staff in the past 12 months. This e-book is packed with regulatory and pharmacovigilance insights from the team at Acorn Regulatory. Download it here.
Acorn Regulatory’s pharmacovigilance and medical teams work with some of the largest and most dynamic companies in the world. They have looked at the major issues impacting their clients at the moment and have created ‘PV Update’ which is our latest PV e-book.
‘PV Update’ considers issues such as:
- An overview of post authorisation safety studies
- The role of the QPPV after Brexit
- What will a UK PSMF look like?
- The increasing obligations of scientific literature
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