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Whether you choose to work directly with us, through a CRO, or bring OmniComm’s suite of eClinical tools fully in-house, our solutions can enhance your CT operations and data management teams. With globally recognized technology, we can help you track and manage your CRO teams, including your existing CRO partner or your expanding network of CRO relationships. OmniComm’s comprehensive portfolio of eClinical solutions will keep your studies on track and on time – across all phases and therapeutic areas.

OmniComm’s suite of eClinical solutions offers a compelling case for delivering oversight, efficiency and excellence to your clinical trials:

  • Reduces cost and time by streamlining study build timelines and enforcing standards across studies.
  • Reuses complex study designs and components across trials leveraging industry standards.
  • Manages data standards for submission.
  • Shares study design using industry standards with related applications, e.g. ePRO.
  • Offers an automated approach to data transfer of SAE data to pharmacovigilance system of choice, which improves compliance and reduces costs by eliminating a need for cross-data reconciliation.
  • Enhances outcomes of RBM and centralized monitoring strategies through the use of a leading auto-redaction technology that enables remote SDV.
  • Automates the entire financial lifecycle of global clinical trials, including contract term translation and contract management.
  • Ensures site investigators are effectively and efficiently trained.

Contact Us      North America +1 877.468.6332      Europe +49 (0) 228 227 440      Click Here to Email Us

Contact Us
North America
+1 877.468.6332
+49 (0) 228 227 440
Click Here to Email Us