ACI CTMS Lite helps clinical research organization (CRO) to optimize study operations, streamline business operations, reduce operational costs and stay compliant by using a modern CTMS system for planning, conducting and monitoring your study.
The Role of ACI CTMS Lite in Clinical Trial Management
Drug and medical device firms conduct clinical trials during the product development process to ensure their products are secure and efficient. Clinical trial management is an expensive, and time-consuming process. If done inadequately, it can result in the collection of inaccurate data that delays time-to-market and also wrecks clinical study subjects. Not surprisingly, the life science industry is turning to technology to enhance the conduct of clinical trials, and to improve transparency into clinical study progress.
Streamlining the document management processes can compromise data quality and participant safety, a proven ACI CTMS solution can help drug & device companies avoid regulatory non-compliance, expedite time-to-market, increase visit reporting productivity up to 40%, and reduce operational costs.
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With decades of expertise in managing data and analytics, and a solid know-how of the processes and requirements of varied industry verticals, we serve businesses of all sizes from several industries.
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