‘Selected Writing from Acorn Regulatory’ Download It 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. 

It looks at a range of issues that are relevant to professionals in the industry, including:

  • Repeat Use Procedures.
  • Pharmacovigilance Audits.
  • Brexit.
  • Scientific Advice Meetings.
  • Patient Information Leaflets.
  • The new 2020 Medical Device Regulations
  • Changes to regulatory demands.

You can download ‘Selected Writing from Acorn Regulatory’ by completing your details below.

Further Reading

Did you know that we produce a wide range of e-books, whitepapers and other publications each year?  Our expert team writes articles of interest to the regulatory, pharmacovigilance and quality community.

You can download some of our publications below.

  1. Deadline 2020:  Are You Ready for MDR?
  2. Regulatory Intelligence 5
  3. Regulatory Intelligence 4

We also publish a monthly newsletter that is filled with useful articles, whitepapers and more.  You can subscribe to the newsletter by clicking here.

Recently, our expert team has written about issues such as:

The update to CMC guidelines

How to apply for a WDA (Wholesale Distribution Authorisation)

and more.  Visit our news and articles page to read more.

 

 

About the Authors
Brian Cleary
Chief Marketing Officer
Brian is Chief Marketing Officer at Acorn Regulatory. He works with our growing team to highlight some of the most important issues in regulatory affairs and pharmacovigilance. Brian also manages HR and recruitment issues for the company. You can read other articles by Brian by clicking the link below.
Other Articles by Brian Cleary
Orla Keane
Medical Devices Manager
An engineer by background, she has 15 years experience in medical devices. Prior to joining Acorn Regulatory, she spent over 12 years at the HPRA in various roles within the medical devices team. She was responsible for a team within post market surveillance and vigilance across various general and active implantable medical device product families. Orla also served as co-Chair of the Compliance and Enforcement working group in Brussels for many years. She has previous industry experience at an orthopaedic implant manufacturer. Orla currently assists Acorn Regulatory clients in a variety of areas including regulatory strategy, EU authorised representative support and preparation for MDR, particularly on the topic of post market surveillance. You can read medical device and related articles written by Orla Keane by clicking the link below.
Other articles by Orla Keane