Emas Pharma

EMAS were established in 1998, initially to enable US biotech and pharma companies to develop medicinal products and medical devices in Europe. From these beginnings, we derived our original name: European Medical Advisory Services (EMAS). Following the success of our European operations, we have expanded our services worldwide and our global and regional operations are now named Emas Pharma. Our mission is to provide support to the pharmaceutical and biotech industry in the development and commercialisation of products worldwide. We also undertake to maintain high quality while retaining flexibility and delivering value to our clients.

Available separately or as part of a comprehensive strategic programme, our Clinical Operations, Regulatory Affairs, Medical Affairs and Pharmacovigilance and Drug Safety groups can provide a tailored package to support you. Emas Pharma global headquarters are based in Hitchin, Hertfordshire, UK. Emas also has offices in Australia, Ireland, Canada, and a US office was in the process of being set-up in California, US.

Our QA department can support you with a range of services including:

- Clinical operations audits

- Investigator site audits

- Pharmacovigilance audits

- System/process and vendor audits

- Regulatory Mock Inspections and preparation and support

- Consultancy, training and mentoring

- Due Diligence (incl. In-licensing & Out-licensing)

- SOP Development

- QMS Development

 

Availability for Work

Worldwide

Areas if Expertise

 GLP, GMP, GCP, GPvP, Computing, GCLP

Contact Details

63-65 Knowl Piece, Wilbury Way, Hitchin, Hertfordshire, SG4 0TY
England

Tel: +44 (0) 462 426 400

Email address: maria.hilling@emaspharma.com

Website: www.emaspharma.com

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