"Everything that's on your mind when it comes to Clinical Research"

About Us

Asian Clinical Trials (ACT) is a full-fledged CRO providing complete solutions for global pharmaceutical, biotechnology and medical device companies in clinical research.  ACT aims to maximize customer value by providing high quality, cost effective, professionalized services. 

Our team comprises of complementary group of professionals representing the fields of Medicine, Nursing, Pharmacology, Microbiology, Toxicology, Statistics, Software Engineering, Business and Law.  Collectively they contribute over 60 years of experience in the drug discovery and clinical development arena, gained in the US, UK and India.  Our staff strength, inclusive of the management team, senior functionaries and support personnel in the clinical operations, data management and administrative staff support provide a  sense of our training, experience, and diversity we bring to the process.

Our team in New Jersey, USA provides seamless project management and customer support with backend operations in Hyderabad, India.

Our full CRO Services includes:

»Study design »Investigator meeting support
» Protocol development »Data management
»Regulatory consulting »Bio-statistics
»Regulatory liaison » Medical writing and clinical study reports
»Project management »Study drug storage and logistics
»Site management »Central lab Coordination
»Site monitoring »Study drug import management
»Adverse event management »Study feasibility support
»GCP Audits »Pharmacovigilance services

Why ACT?

»  Experience in conduct of studies from Phase I thru phase IV .

»  Excellent relationship network with investigators in India.

»  Costing models that are competitive and comparable.

»  Solid experience, expert guidance and robust technology.

»  Ability to adapt to meet project specific scope and timelines.

»  Strict adherence to GCP guidelines, USFDA and Indian regulations.

                   " ACT now... for Quality Clinical Research Services"