Our Global Presence for Your Global Trial

Drug development has been globalized, and Multi-Regional Clinical Trials (MRCT) for regulatory submission have widely been conducted by global biopharmaceutical companies with the objective of leveraging the global clinical trial resources and reducing the time lag of launch in key markets for the benefit of patients around the world.

With a global presence of more than 4,000 employees across 20+ countries in 80+ cities, we are capable of conducting MRCTs for pharmaceutical, biological, natural medicine and medical device studies across Asia, Europe, North America, Southeast Asia, Australia and New Zealand, supporting our clients’ global innovation to the most extent.

Full Service Provider for MRCTs

ClinChoice is equipped with two specialized teams to support our clients’ global innovation in the key markets: Asia-Pacific region (ClinChoice APAC) and North America and Europe region (ClinChoice International). We can provide our clients with expertise and full services of project management, clinical operations, biometrics, medical, regulatory, drug safety, quality, site management, bioanalytical lab, technology platforms as well as FSP, to meet our clients’ various development needs.

Global Program Management Office (GPO)

A global team with experienced project managers from North America, Europe Union, China, Japan, Southeast Asia, Australia and New Zealand to facilitate the delivery of MRCTs

A Steering Committee with top management across regions to closely oversee the delivery of MRCTs, and provide a unique level of C-Suite availability, attention and resources not commonly found in the industry.

Streamline the cross-border regulatory, ethical and operational requirements and procedures to achieve quality and success in studies while keep efficiencies in time and budget

Global Project Management (GPM)

A main point of contact with sponsors, regional PMs, functional team leads and vendors

A GPM team with global presence in North America, Europe Union, China, Japan, Southeast Asia, Australia and New Zealand with world-class project management experience

Oversee and maintain the study timeline, budget and quality, and manage the challenges strategically

Harmonize study procedures across countries/regions to ensure consistent standards are followed globally

Provide customized regulatory, ethical, operational strategies and solutions to achieve study feasibility locally

Facilitate a seamless communication to overcome language barriers and cultural differences