Pharmaceuticals / Biotechnology

Non-clinical development capabilities:

15+ years experience within various pharmaceutical/CRO settings covering small molecular entities, vaccines, large molecules/biologicals and medical devices; 

Proficient in the design, preparation and implementation of in vivo and in vitro studies related to all non-clinical development activities;

Expertise across various therapeutic areas, including numerous modes of administration and various animal species;

Available services include:

  • Single point of contact in monitoring and coordinating outsourced studies;
  • Author non-clinical safety sections of Briefing Documents, Investigator Brochures (IB), Investigational New Drug (IND) and Clinical Trial (CTA) applications;
  • Regulatory non-clinical queries.

Contact us for more information regarding our services