Science-driven approach to assist in shaping any aspect of your clinical development strategy

We provide a team of subject matter experts to support, tailor and lead your study and advise you on the optimal directions from the design of your clinical trial to the delivery of meaningful & high-quality results.

Medical and Scientific Affairs (all Phases)

StrongCORE Scientific contribution Maximize the value of your clinical development program with our flexible, fit-for-purpose consulting solution called StrongCore Scientific (SCS) and gain access to a multidisciplinary team of experts which is always uniquely composed, members are selected and involved in harmony with the special development needs.

We provide you our regulatory, statistical, medical and translational science experts with high qualifications and practical in-depth knowledge of the therapeutic area to plan and lead your study, who understand your needs, the associated challenges and opportunities in your study, interpret data in its real context, tailor the project strategy and advise you concerning the optimal strategic direction at any stage of the study.

Through our StrongCore Scientific (SCS) group you will gain access to a multidisciplinary team of experts, consists of Accelsiors’ subject specialists and consultants from various professional fields with advanced educational and professional background in life sciences, significant experience and expertise across the entire drug development industry. StrongCore Scientific is a flexible, fit-for-purpose consulting solution, the team is always uniquely composed, members are selected and involved in harmony with the special development needs.

We provide consultancy services for Pharma and Biotech companies in the support of
Feel free to ask Accelsiors’ Medical and Scientific experts!

Let’s start discussing about how we can support your pipeline! Please, contact us:

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  • Orphan Designation
  • Clinical strategy
  • Regulatory strategy: support to the different expectations of the European (EMA), US (FDA), and many other regulatory agencies around the world
  • Pediatric Investigational Plan
  • Biomarkers Validation
  • PopPK
  • PK/PD modelling and simulations
  • Study design, statistical considerations
  • Protocol review
  • Clinical development plans
  • Risk assessment and SAE/AE review
  • Medical monitoring plan and 24/7 medical monitoring
  • Medical writing

Learn more about our comprehensive clinical development services

Accelsiors offers a complete range of expertise in support of your specific needs: Scientific, analytical and regulatory complemented by global resources, state-of-the-art technologies and project management methodology for the most effective execution of your development program across all phases of clinical drug development.