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A-consult Group celebrates Big Four Oh
Copenhagen in Denmark and Grasse in France: A-consult Group and A-pharmaconsult, the consultancy that specializes in regulatory and quality services for pharma industries and medical devices, celebrated its 40th Anniversary during April 2023.
From the company’s headquarters in Copenhagen, its CEO Bjarne Alstrøm said: “I am happy to announce that A-consult Group today has been in business for 40 years. Thank you to all clients and employees who are or have been part of our journey and made it possible.”
M. Loïc Girot, General Manager in Grasse – France, said that A-pharmaconsult was looking forward to further expanding its regulatory services to pharmaceutical industries, alongside quality services, against a background of ever increasing pharma industry need.
M. Girot commented: “We have seen particular demand for our services associated with switch of Technical Documentation from MDD 93/42 to MDR 2017/745 for CE marked Medical Devices, along with difficulties in regulatory compliance for medicines.”
A-pharmaconsult traces its roots back to the 1983 founding of Alstrøm Consult company (A-consult Group) in Copenhagen as a specialist in regulatory services within dietary supplements and programming solutions to data companies. Since then it has progressively extended into more general pharma consultancy, recruiting a very strong team of pharmaceutical consultants, programmers and IT specialists.
In 2003 the company, A-consult Data ApS, was founded to manage all data services and two years later, A-consult expanded its international operations by acquiring the French pharma consultancy Yarra SAS to form A-pharmaconsult SAS, with Loic Girot becoming its General Manager in 2007.
The company’s technical and medical writing services ensure correct drafting, updating, filing and monitoring of technical documentation for medical devices and marketing authorization dossier for medicines in accordance with current regulatory and normative requirements.
It also provides audits of manufacturing plant according to ISO13485:2016 or cGMP and internal audits based on ISO13485:2016 or cGMP.
About A-pharmaconsult SAS
Part of the A-consult group, A-pharmaconsult SAS specializes in regulatory affairs for medicines and medical devices.
A-pharmaconsult services include medical writing, non-clinical writing, technical writing, regulatory strategy, and quality systems. These offerings include preparation of marketing authorization dossiers for drugs, technical documentation for medical devices, regulatory consultancy and documentation for quality management systems (GMP, GDP, ISO 13485 & ISO22716).
From both its Danish and French origins, this consulting company has remained deeply focused on helping pharmaceutical, medical devices and cosmetics businesses operate in an increasingly complex regulatory environment, underpinned by core values of expertise, respect, and confidence.
A-pharmaconsult has built long term partnerships across a broad range of different companies with a “tailor made” offering to suit every size of company and specific needs.
For more information, visit www.a-consult.com
Click on A-consult Regulatory Affairs Services for background information.