Acorn Regulatory

From Verify.Wiki
Jump to: navigation, search

Acorn Regulatory is an ISO-certified medical device and pharmaceutical consulting firm that specializes in assisting companies with European regulatory approvals and quality assurance.

QuickUpload1085 20170603064608.png
https://acornregulatory.com/
Acorn Regulatory
Industry Pharmaceutical

Medical Devices

Pharmacovigilance

Founded 2002
Headquarters Suite 6 Powerstown House

Gurtnafleur Business Park, Clonmel, Co. Tipperary, Ireland

History

1. Since 2002, Acorn Regulatory has been synonymous with success in its field. In almost 15 years, they take pride in never receiving a rejection from a Competent Authority. That’s a 100% success rate! Client testimonials are readily available on our corporate website.

Acorn Regulatory is an ISO-certified medical device and pharmaceutical consulting firm that specializes in assisting companies with European regulatory approvals and quality assurance. Our practice areas include:

  • 2.Pharmaceutical (including regulatory affairs)
  • 3.Medical Devices (including regulatory affairs)
  • 4.Pharmacovigilance
  • Clinical Trials Services
  • WDA Services
  • EU Authorised Representative
  • Known as eCTD experts.
  • PV Auditing

Services include:

Acting as the EU Authorised Representative Wholesale Distribution Authorisations Advertising Compliance Review of medicinal products Resourcing and Outsourcing of Regulatory Affairs Specialists Acorn Regulatory is headquartered in Tipperary, Ireland. Their team is one of the most experienced and highly regarded regulatory affairs teams in Europe. They have, over the course of their careers, worked on myriad projects for healthcare companies of all sizes. The team continues to grow at their offices in Ireland and with their staff on client sites throughout the world. The company has 100% compliance with the reporting timelines in relation to the reporting of adverse reactions as individual case safety reports (ICSR) (https://acornregulatory.com/what-we-do/pharmacovigilance/). Routine literature reviews, PV auditing, electronic reporting, and pharmacovigilance training are services offered by their pharmacovigilance division.

Controversies

Top 5 Recent Tweets

DateAuthorComment
December 14, 2018Acorn_RegRegulatory Affairs Case Study - Moving to OTC https://t.co/cRg0smUkxg https://t.co/4gpTFGAgC3
December 14, 2018Acorn_RegWant to find out more about the roles we have and how we offer a greater degree of work flexibility than other comp… https://t.co/jDjGjLcgRN
December 13, 2018Acorn_RegOur end of year newsletter has a free e-book and much more. Get it here: https://t.co/9aETKuMp1G https://t.co/YQOGsi7W4z
December 12, 2018Acorn_RegIn our end of year series we are looking at the most widely read articles on our website. Here, we are looking at… https://t.co/bA7TphVN8Q
December 12, 2018Acorn_RegChristmas jumper day at Acorn Regulatory! https://t.co/cuk7Fjpzqq


References

  1. https://acornregulatory.com/
  2. https://acornregulatory.com/what-we-do/pharmaceutical/
  3. https://acornregulatory.com/what-we-do/medical-devices/
  4. https://acornregulatory.com/what-we-do/pharmacovigilance/
  5. https://acornregulatory.com/whoweare/heres-clients-say-us/

Verification history