Advance your clinical development program faster with Clinpacific life science solutions.

Clinpacific life science solutions offers comprehensive services ranging from project management to clinical trial monitoring, oversight, and patient recruitment. As a leading CRO in the North American region, it brings exceptional expertise and in-depth knowledge of local regulatory requirements.

Clinpacific life science solutions is a top clinical trial provider in the North American region, offering efficient and cohesive trial services through expert teams with extensive industry and therapeutic knowledge spanning all phases of clinical development.

The teams maintain strong connections with trial sites, key opinion leaders, and Principal Investigators, enabling swift and efficient trial initiation, patient enrollment, and site selection to ensure clinical timelines are met.

Exceptional client satisfaction

Clinpacific life science solutions has established a structured approach to monitoring customer and investigator satisfaction across various aspects of our work. We’ve invested in advanced technology and set up defined processes to consistently engage with clients at key project milestones. This initiative plays a vital role in strengthening client relationships, proactively identifying potential concerns, and driving continuous service improvement. Overall, we’ve seen outstanding satisfaction levels, particularly in areas like communication and the quality of our project teams.

Comprehensive Project Management solutions.

1. Site feasibility evaluation and selection
2. Protocol design and CRF (Case Report Form) development
3. Strategic patient recruitment planning
4. Submissions to Ethics Committees and regulatory authorities
5. Project oversight and monitoring for Phase I–IV clinical trials
6. Comprehensive biometrics support, including randomization and IWRS solutions
7. Local sponsor representation
8. Coordination and management of third-party vendors
9. Medical, technical, and clinical study report (CSR) writing

Site oversight and management (SMO) services

Clinpacifics life science solutions experienced and skilled study coordinators and site management associates play a crucial role in the successful execution of clinical trials.

Through its Site Management Organization (SMO) service, Greenline Clinical Research offers highly qualified Study Coordinators (SCs) and Site Management Associates (SMAs) to support both principal investigators and sponsors.

This SMO service equips principal investigators with trained SCs to assist in managing daily clinical trial operations and patient recruitment, while providing sponsors with seasoned SMAs for site management and ethics committee support.