#RegulatoryClinicalDevelopment

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Clinical Data Management Services

CDM (Clinical data management) services professionalized in clinical trial management services, more specifically management of the clinical trial process, patient recruitment resource management, including site performance, operational planning, contact information, and regulatory document recordkeeping.

Companies that conduct clinical trials, Medical device manufacturers, Pharmaceuticals and Biotechnology companies, and university or governmental research organization uses this kind of software system which is good at managing clinical data.

There are many clinical data management services like On-shore and Off-shore clinical data management, CRF/eCRF design and development, CRF annotation and reviews, Database build and design, Medical coding, Real-time data viewing, and reporting, etc.

The clinical data management systems must have below mentioned attributes and also FDA guidance contains these fundamental elements of data quality for both paper and electronic records.

It should be Attributable, Legible, Contemporaneous, Original, Accurate, Readily available, Transmissible, Storable and most importantly data must be complete and unbiased.