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Early-Phase Clinical Studies Worldwide
 
Phase II to IV Clinical Studies Management and Monitoring
 
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Medical Devices

TransCom Global Ltd. is a one-stop-shop Contract Research Organization highly experienced in designing and executing medical device studies. TransCom specializes in both medical device studies as well as combined studies of medical devices and drugs. We are experts in the regulatory requirements, and conduct periodic meetings with Regulatory Authorities to streamline approval processes, ensuring an errorless design and quick approval for our clients' clinical trials.

 

TransCom's experience in Medical Devices

  • Our medical device's experienced and dedicated staff ensures the highest quality for our clients
  • TransCom seeks a long-term relationship with our clients, starting from the end of pre-clinical phase through First-in-Human (Pilot) to Pivotal studies for CE Notification/510(k) or CE Mark/PMA
  • TransCom's reputation as medical device experts stems from our ability to significantly enhance our clients' chances to reach their development and financial goals.
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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