At Emas Pharma we support the Pharmaceutical and Biotech industry in developing and commercializing products worldwide. We believe in providing the highest quality service, whilst always delivering value; a mantra that we have never deviated from.
We help drive pharma and biotech product development from first into man to the end of the product lifecycle. We can support individual projects or complete development programs and everything in between through our expert functional groups: Clinical Operations, Pharmacovigilance / Drug Safety, Regulatory Affairs, Medical Affairs, Strategic Consultancy.
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 about Clincal Operations →
Whether it's for short term-projects such as preparation of a periodic safety update report (PSUR), through to long-term projects such as establishment and operation of a drug safety system to support your clinical trials and/or marketed products.
Emas Pharma provide a variety of pharmacovigilance services to suit your needs.Read more about Drug Safety →
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 about Regulatory Affairs →
Successful commercialization depends on creating, interpreting and communicating data so that it is meaningful and resonant to the target audience.
We harness our comprehensive international experience and expert knowledge to advise and implement strategies to maximise the commercial potential of your product right from the early phases of development all the way through to lifecycle management.Read more about Medical Affairs →
Our strategic consultancy group have global, regional and national expertise in drug development and commercialisation. We have the experience to see things from big pharma, small pharma, biotech and regulatory authority perspectives.
The Strategic Consultancy group provides senior medical oversight to our internal teams in Drug Safety and Clinical Operations and also offer high level Regulatory Affairs and Medical Affairs services.Read more about Strategic Consultancy →