We’re proud to be different from other CROs, and nothing highlights this more than our clinical division.

Our in-house team of clinical experts support over 70 countries to undertake studies needing specialist requirements, working seamlessly with our other full-service in-house divisions in regulatory, medical, pharmacovigilance and quality assurance.

Strategic Clinical Development

Our experienced team of experts can provide:

  • Clinical development plans

  • Investigator brochures and protocols

  • Study feasibility, including KOL and site identification

  • Informed consent/patient information leaflets

  • eCRF data management development

  • Investigator meetings

  • Site contracts and budget negotiations

  • Ethics submissions and local approvals

  • Study drug import and management

  • Identification and oversight of study service vendors (e.g., central and specialist laboratories)

Clinical Study Initiation

Product development strategy and planning with full-service support for Phases I-IV of clinical trials.

Clinical Study Initiation

  • Full clinical trial site management

  • Global project management

  • Data management and statistical analysis

  • Data safety monitoring board (DSMB)/data monitoring committee (DMC) setup and management

  • Trial master file (TMF) and eTMF services

  • Risk-based monitoring (RBM)

Get In Touch

Our team is ready and willing to support your clinical needs.

To discuss your specific project requirements, contact us today.