The Bionical Emas difference is that ‘To Care’ is part of our culture and founding philosophy. We care about delivering for our clients, the investigator sites with which we work every day and we care about the patients whom we ultimately serve. We care about the quality of the work we produce, and we care that our staff are supported, so they deliver the best they can, each and every day. Contact us and let Bionical Emas care for your clinical development plans.
We can support you with.
Our systems, processes, and training are built around an integrated platform of seamless quality project delivery
All clinical research activities, from clinical trial applications through to project management and monitoring, are conducted by our highly experienced team
Regulatory & HE Science
We know how to overcome hurdles for routine or complex and unusual therapies in all key regions and in unfamiliar countries
We understand that pharmacovigilance regulations are complex and constantly evolving and will ensure that you are fully compliant with all requirements
At Bionical Emas our data services are tailormade to meet the needs of individual clients
Our processes, systems and training are built around our comprehensive Quality Management System (QMS)
We have a highly experienced team of scientific, medical and compliance reviewers, including final medical signatories, and we can provide 24/7 Medical Monitoring cover and Medical Information services
- From kick-off meeting to SIV in five days – a severe COVID-19 pneumonia case-study Explore
- Effective Pharmacovigilance & Regulatory EU and Australian Due Diligence, leading to operational and consultative support Explore
- Bionical Emas Regulatory Affairs: Mutual Recognition Submission Strategy Explore
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