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Clinical Operation

About service

Based on accumulated know-how and expertise, C&R Research provides clients with specifically developed services for late phase clinical trials including phase IV trials, observational study, registries, and post-marketing surveillance (PMS) studies.


Study Design

Pre-Study Visit

Regulatory and IRB Affairs

Site Contract

Materials Development

Initiation Visit

In-House Site Management

Essential Document Management

Regular Monitoring Visit

Close-Out Visit

SAE Affairs

Project Management

Dedicated LPS (late phase service) team with comprehensive insights

C& R Research’s LPS team of professionals, including highly experienced CRAs (CRA I, CRA II) and project managers with years of clinical experience and expertise in many therapeutic areas, has annually carried out several tens of projects. It can be safely said that LPS team is one of the most competitive teams within C&R Research, posting more than 20% growth in annual sales. Under clients’ full recognition, LPS team continues to provide reliable services based on accumulated experience and expertise.

Rapid, accurate LPS via smooth communication system and SOP

For efficient operation of a client’s individual projects attuned to their features, the standard operating procedures (SOPs) of C&R Research are applicable to non-interventional study (NIS) and PMS studies. Based on smooth communication with other business units (Data Management, Biostatistics, Medical Writing) and relevant SOPs, you can be assured of C&R Research’s rapid and accurate LPS customized to intended purpose of each project and to the needs of clients.

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