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Early-Phase Clinical Studies Worldwide
 
Phase II to IV Clinical Studies Management and Monitoring
 
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Our Company Culture

ATTITUDE

We attach great strategic importance to our partnership attitude towards our clients. We select our staff based on knowledge, experience and attitude as the most important criteria. As part of our strategy, we ensure that our staff’s attitude is aligned with the company’s values on an ongoing basis.

 

QUALITY

TransCom attaches the highest importance to Quality Assurance and our organizational culture instills the values of high-quality standards in each and every employee.

 

COMPLIANCE WITH CLINICAL TRIALS REGULATIONS

All procedures at TransCom are conducted in compliance with both the ICH-GCP guidelines, local regulatory requirements, and client-specific SOPs and requirements.

 

CONFIDENTIALITY

TransCom insists on strict confidentiality for all client information and documents in order to safeguard Intellectual Property rights.

  • All staff sign a non-disclosure agreement and, if required, a client NDA as well
  • Each project team has access only to their own projects
  • All disposable hard copies are shredded
  • TransCom has a high-spec computerized security system
     

 

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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