As a leading global provider of outsourced development and REACH services to the pharmaceutical, biotechnology, chemical and medical device industries, we help clients manage their regulatory affairs in a cost effective and timely manner. ELC GROUP has significant experience in helping clients understand the regulatory requirements for the development of pharmaceuticals and medical devices covering everything from strategic development planning to market registration.
elc group delivers its customized solutions through its four core business segments:
- Regulatory Affairs Services
- Global Regulatory Consulting for Medical Device and IVD Companies
- EU REACH (Registration, Evaluation and Authorization of Chemicals) Regulation Services
- Corporate Languages Solutions (Translations, Design, DTP, Localization)
The benefits we bring to our client partners are numerous:
- Exceptional industry knowledge and experience at competitive pricing
- Superior leadership team abreast of all current industry trends, and continuously directing company initiatives toward solutions to market challenges
- A large, deeply talented project management team to ensure expedited project results without sacrificing quality
- Constant focus on communication enabling stronger client project participation and control
- Strength of diversity – our team is made up of over 15 different nationalities
- Peace of mind from knowing you have found the right partner!
Specialties
Regulatory Affairs Services, Global Regulatory Consulting for Medical Device and IVD Companies, Language services and Translations, DTP, REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals), EVMPD software




