Clinartis is a dynamic contract research organization (CRO) serving pharmaceutical, biotech and medical device companies to support Phase I - IV drug and device

We offer consultation and training on compliance with Medical Device Regulation around the world and standards including ISO/EN 14971 (risk management), the IEC/EN 60601-1 series.

We offer consultation and training on compliance with Medical Device Regulation around the world and standards including ISO/EN 14971 (risk management), the IEC/EN 60601-1 series.

We offer consultation and training on compliance with Medical Device Regulation around the world and standards including ISO/EN 14971 (risk management), the IEC/EN 60601-1 series.

Clinical Research Consultants is a clinical and regulatory affairs CRO, based in central Paris, is particularly focused on compliance to moral, legal and scientific integrity, of clinicalresearch worldwide.

Botique engineering firm in Denver, Colorado for the Energy Industry

We offer consultation and training on compliance with Medical Device Regulation around the world and standards including ISO/EN 14971 (risk management), the IEC/EN 60601-1 series.

Maintaining up to date global regulations is a costly task. Aside from sourcing legislation from different vendors, databases and government agencies, the effort involved in digesting the regulations into usable requirements and test methods for product

PROVIDING A BRIDGE BETWEEN RESEARCH AND REGULATIONS GLP Support Services was started as a consultant/contractor service company providing GLP auditing services to the pharmaceutical industry.  Since its inception in 2002 our client base has expanded to in

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PharmApprove, a leader in FDA advisory committee preparation and strategies, is a strategic regulatory and drug communications consulting partner. PharmApprove helps teams create the strongest case to the FDA advisory panel and the EMA for their drug, dev

Your complete Life Sciences Meeting Support solution: investigator presentations, FDA Advisory Committee (AdComm) preparation and EMA Oral Explanation support.

Your complete Life Sciences Meeting Support solution: investigator presentations, FDA Advisory Committee (AdComm) preparation and EMA Oral Explanation support.

Set up by a former FSA Permissions Case Officer - we offer a door-to-door service to get your business Authorised - 01604 76 22 33

SKP is a leading professional services group in India providing sound business and tax consulting and accounting services to international companies currently conducting or initiating business in India as well as those expanding overseas.