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An Asia-Pacific based, ICH-GCP compliant CRO offering a complete range of clinical research and new drug development services. APEX is familiar with regulatory requirements for implementing clinical trials in Asian countries.

Indian CRO designs and conducts Clinical phase II to IV trials for pharmaceutical, biotechnology, and medical device companies without compromising on ICH-GCP standards.

An independent full-service CRO offering GCP clinical research services in India. Clinical trials in India offer rapid enrollment, treatment naive patients, and economically favorable costs.

A Pan-Asian Site Management Organization (SMO)and Contract Research Organization (CRO) headquartered in Singapore. Includes a clinical research network of over 40 sites located in Singapore, Malaysia, Indonesia, Thailand, Vietnam, Philippines, Mainland China, Hong Kong, Taiwan, India, Australia and New Zealand

International CRO services based in Istanbul, Turkey.

A Taipei-headquartered CRO providing ICH-GCP compliant clinical trial management(Phase I~IV), bioequivalence and pharmacoeconomic studies, botanical drug R&D and central laboratory services.

Full service CRO based in India works with pharmaceutical companies to conduct clinical trials in various therapeutic areas

Indian CRO Provides a broad range of Phase I clinical research services including bioavailability, bioequivalence and pharmacokinetic studies in their new clinical research unit.