We bring decades of experience in developing and commercialization medicine at global, regional, and national levels. We drive pharmaceutical and biotech product development from first into man right the way through to the end of the product lifecycle. To understand the needs of our clients and suppliers, we speak with them, not at them and this is evident as most of our work is repeat business.
In November 2016 Emas Pharma became part of Bionical, bringing full service Clinical Research services to the Bionical group of companies. To learn more about Bionical please visit the website.
All clinical research activities, from clinical trial applications through to project management and monitoring, are conducted by our highly experienced team. Our vast experience has ensured the successful delivery of numerous projects across all phases of clinical development, from first–in-man to post- marketing surveillance studies.Read More
Our Clinical Trial Supply services provide unrivalled global access to medicines and ancillaries for use in clinical trials. Whether it be for use as a comparator, co-med, rescue therapy or ancillary supply, our global network of manufacturers and authorized distributors, underpinned by our market-leading Quality Management System, enables us to provide a customized end-to-end supply solution for our clients.Read More
Our Early Access Programs (often called Pre-approval Access, Compassionate Use, Named Patient, Expanded Access, Managed Access Programs) deliver lifesaving treatments to patients around the world, whilst adding true value to our clients through a range of in-house additional cutting-edge services.Read More
Emas Pharma have a highly experienced team of scientific, medical and compliance reviewers, including final medical signatories. In addition, the services span out to provide 24x7 Medical Monitoring cover and Medical Information services.Read More
Our team of dedicated pharmacovigilance professionals can cover all your pre- and post-approval pharmacovigilance requirements from case processing, global regulatory reporting and aggregate report preparation through to full service clinical trial or post-approval systems including signal detection, literature review and QPPV provision.Read More
We know how to overcome hurdles for routine or complex and unusual therapies in all key regions and in unusual or unfamiliar countries. Our regulatory team is responsible for numerous successful submissions to major competent authorities and regulatory agencies. Our skilled teams develop high-quality written documents that are compliant with global and national regulatory requirements.Read More
We have a wealth of experienced professionals who can support your QA needs from conducting audits through to complete development of a Quality Management System. No problem is too big or too small.Read More
At Emas Pharma our people are dedicated to the success of the projects they manage. They are passionate about what they do. Our teams work together to deliver the professional service our clients require. As an organisation we are committed to recruiting scientifically qualified individuals who are professional and work to high ethical and moral standards.
We are interested in meeting positive and enthusiastic candidates who can contribute to our organisations success.
We will endeavour to respond to your enquiry within 24 hours.Contact us
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