Clinical Service Center (member of ACROSS Global group)

Your Trustworthy CRO - CSC：A leading expert in the field of clinical trials"
Clinical Service Center ia a full-service CRO which was established on Dec. 2008. CSC is headquartered in Suzhou, and branch offices in Beijing, Shanghai, Guangzhou,Xi’an, Nanjing, Shenyang, Tianjin and Chengdu, etc. As our reputation grew, so did our international clientele. CSC has transformed from a solely local CRO to a CRO with offices outside of Mainland China, our oversea offices includes: New York, Toronto, London and Taiwan. CSC can provide professional clinical services to sponsors worldwide, and dedicate to improve the standards of healthcare across the world. CSC actively participates in clinical services cover wide range of therapeutic areas worldwide, provide professional clinical trial services to pharmaceutical companies, academic institutions, clinical research institutions, experts and clinicians. CSC has been positioning at the forefront of the industry. We provide high quality and efficient clinical trials services that comply with ICH-GCP and CFDA relevant regulations to our clients.

Our service

Regulatory Affairs ,Clinical Monitoring & Project Management, Data Management, Statistical Analysis & Statistical Programming, Pharmacovigilance Quality Assurance Medical Writing / Medical Affairs Site Management (SMO) 
In addition to these core services: We can help you identify investment and/or partners in China through our Partnership Database

Our strengths:

l Stable & Professional Team:  A large geographical coverage, Average of 3 years experience in the industry Professional, customer-orientated and GCP trained
l Clinical Expertise: We have worked on hundreds of clinical trials across all stages of development in a wide range of therapeutic areas. Through our work we have established a vast database of information regarding clinical sites and investigators in China, as well as a strong network of relationships with local KOL.
l Knowledge of the Local Market: We know China – its people, culture, regulations and quirks. We know where the obstacles are and how to overcome them. We know where the opportunities are and how to take advantage of them. Outside of clinical research we can also help you if you are looking for investment, partners and market information.Has an international first-class data management system. Global quality standards at a local (competitive) prices: Our SOPs meet the requirements of ICH-GCP/FDA 21 CFR part 11, we have a robust quality assurance and training system and the majority of our management staff have worked in either Big Pharma or Global CROs, and have ample experience conducting global clinical trials.