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Early-Phase Clinical Studies Worldwide
 
Phase II to IV Clinical Studies Management and Monitoring
 
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About Us

TransCom Global, established in 1998, is a CRO focused on providing customized, budget optimized clinical trial management services.

We specialize in managing clinical trials for the Pharmaceutical and Biotechnology industries,  and have vast experience in working with Medical Device companies. 

Our main goal is to provide a unique and successful infrastructure for the management and monitoring of clinical trials, to support our clients from late pre-clinical to late clinical development stages.

Since TransCom was established, we have consistently justified the confidence of our customers in the pharmaceutical, biotechnology and healthcare industries by demonstrating a company-wide commitment to meticulous precision, unsurpassed quality, timely service and value pricing.

TransCom Global has been managing clinical studies since 1998, and we provide the following service offerings to our clients:
 

  • Design, Monitoring, site management and project management for national and multinational clinical trials, in all therapeutic areas including medical devices (phase I-IV).
  • Patient Reported Outcome (PRO)  Neuropsychological Validation for Multicultural Clinical Studies
  • Preparation of Multilanguage Regulatory Documents for Clinical Studies Worldwide
     
Preparation of Multi-Language Regulatory Documents for Clinical Studies Worldwide
 
Patient Reported Outcome (PRO) Neuropsychological Validation for Clinical Studies
 
Our Clients
Leading CROs, pharmaceutical, medical device and biotech companies

 
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