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Health care and medical technology servi


Clinical Trial Management System CTMS allows pharmaceutical companies, biotechnology companies, and contract research organizations (CROs) to better manage the clinical trial process, maintain quality of clinical trials, and manage investigator relationships. It provides a comprehensive set of tools for clinical research associates (CRAs), clinical investigators, and site coordinators, including a personalized Internet portal to conduct study activities more efficiently.

The CTMS solutions are rapidly undergoing technological advancements. Lack of skilled professionals is pushing pharmaceutical and biotechnological firms to invest in training programs to make them familiar with various aspects of sophisticated solutions. Furthermore, costs of these systems are high owing to their ability to integrate a wide range of capabilities. Thus, high cost associated with CTMS is anticipated to hinder the adoption by small and medium-sized companies. The global Clinical Trials Management System (CTMS) market size was valued at USD 592.07 million in 2016. It is anticipated to expand at a CAGR of 12.1% over the forecast period. 


Managing clinical trials can be difficult with numerous moving parts, complex protocols, and large amounts of data, having clear oversight and the ability to streamline trial operations is critical to a study’s success.


IKCON PHARMA  provides staffing/services/solutions in implementing Bioclinica CTMS, Oracle Siebel CTMS, Paraxel IMPACT CTMS, Veeva CTMS, Medidata CTMS systems. We also provide services/staffing services for small and mid-sized companies who would like to implement CTMS solutions with less cost and effective results.Support implementation of the following key process areas/modules:

  • Program Management

  • Protocol/Study Management

  • Account Management

  • Contact Management

  • Country Management

  • Site Management

  • Subject Management

  • Site Monitoring

  • Track Milestones

  • Site Contracts

  • Site Payments

  • Document Tracking

  • Reporting & Analytics

  • Administration

  • Configuration

  • Audit Trial

  • GxP Assessment

  • 21 CFR Part 11 Assessment

  • Validation


  • System Type

  • Enterprise

  • Site

  • Delivery Mode

  • Web-based

  • Cloud-based

  • On-premise

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