03.08.24 -- Find Consulting And Regulatory Partners For Your Clinical Trials

Phlexglobal’s unmatched expertise working in any eTMF system is enabling teams to assess, prevent, and manage risk across the entire TMF spectrum – improving inspection-readiness with less effort. You can choose a single offering, several, or end-to-end.

Novotech is recognized as the Asia-Pacific full-service CRO. Novotech has been instrumental in the success of over 1,000 clinical trial projects in key areas such as immuno-oncology, infectious diseases, vaccines, and orphan and rare diseases.

IQVIA's end-to-end Local Affiliate Product Services (LAPS), with safety-focused industry experts and latest technologies, ensure global consistency at a local country level and compliance with all local safety requirements.

Veristat’s regulatory publishing team offers extensive expertise across the full scope of regulatory requirements, including your applications, amendments, supplements and reports to the FDA through the Electronic Submissions Gateway (ESG).

Are you still in doubt about your study protocol or how to determine the sample size? Gain access to free clinical trial budgeting and MedSci consulting services from a leading Eastern European CRO, regardless of the stage of your project.

At YPrime, we streamline your clinical trial journey, increasing certainty from study design to data lock. With nearly two decades at the forefront of clinical trials, we look ahead and design research studies to minimize challenges and solve for certainty.