Acorn Regulatory
Acorn Regulatory is an ISO-certified medical device and pharmaceutical consulting firm that specializes in assisting companies with European regulatory approvals and quality assurance.
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| 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
| Date | Author | Comment |
|---|---|---|
| August 23, 2019 | Acorn_Reg | What are the responsibilities of an EU Authorised Representative? If you need to appoint a new EC Rep you should ta… https://t.co/Uv2NEdhUc7 |
| August 22, 2019 | Acorn_Reg | 2019 Pharma Awards Finalist - Acorn Regulatory Shortlisted https://t.co/kAdLZCvVEY |
| August 19, 2019 | Acorn_Reg | 'Selected Writing from Acorn Regulatory' Download It Here https://t.co/P5rihLloio |
| August 16, 2019 | Acorn_Reg | This article looks at applying for a marketing authorisation for a pharmaceutical product. Acorn Regulatory can hel… https://t.co/ukHraQMT9x |
| August 16, 2019 | Acorn_Reg | Want 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/DH8DubRjiG |
References
- https://acornregulatory.com/
- https://acornregulatory.com/what-we-do/pharmaceutical/
- https://acornregulatory.com/what-we-do/medical-devices/
- https://acornregulatory.com/what-we-do/pharmacovigilance/
- https://acornregulatory.com/whoweare/heres-clients-say-us/
Verification history
447 days ago
472 days ago- 639 days ago
- View all verifications
