Acorn Regulatory Consultancy Services Limited

Expertise You Can Trust.

General Information
Company Name
Acorn Regulatory Consultancy Services Limited
Founded Year
2002
Location (Offices)
Ireland
Founders / Decision Makers
Number of Employees
20
Industries
Medical Devices, Pharmaceutical
Funding Stage
-
Social Media

Acorn Regulatory Consultancy Services Limited - Company Profile

Acorn Regulatory Consultancy Services Limited is a leading regulatory affairs consultancy with a strong focus on Pharmaceutical & Medical Device Regulatory Affairs and Pharmacovigilance. Since 2002, the company has been providing expert assistance to a wide range of companies, supporting them throughout various stages of growth. Its extensive range of services includes regulatory applications, expert report writing, due diligence reviews, electronic submissions, and compliance maintenance in the pharmaceutical sector. Moreover, the company offers Pharmacovigilance services such as QPPV services, electronic reporting, signal detection reports, and routine literature review. In the medical device field, Acorn Regulatory provides CE Mark Certification, European Authorized Representative Services, ISO 13485 Certification, and Medical Device Training Programmes. Based in Ireland, the company prides itself on its ability to seamlessly integrate into existing team structures and meet regulatory requirements with minimal training time. Acorn Regulatory's tailored solutions cater to both short and long-term regulatory and compliance needs, enabling companies to operate with maximum efficiency and confidence. With a proven track record, the company has established itself as a reliable partner for those seeking the highest quality regulatory and compliance support in the pharmaceutical and medical device industries. For more information, interested parties can reach out to Acorn Regulatory via phone at +353 52 6176706, email at [email protected], or by visiting their official website at www.acornregulatory.com.

Taxonomy: Regulatory Affairs, Pharmaceutical Regulatory, Medical Device Regulatory, Pharmacovigilance, Global Regulatory Strategy, Electronic Submissions, CE Mark Certification, ISO 13485 Certification, Medical Device Training Programmes, Qualified Person for Pharmacovigilance (QPPV) Services, European Authorized Representative Services, Post-Marketing Surveillance, Signal Detection Reports, Therapeutic Categories

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