Clinical Data Management

The process of gathering, storing and curating copious volumes of clinical data is deemed to be very intrinsic from the perspective of regulatory compliance. GVR BIO SCIENCE is a contract research organization engaged in full-fledged and knowledge-based services and offers clinical data management solutions.

organisation (CRO), biostatistical services have always been a key component of Quanticate's services as part of our heritage. Our biostatisticians have a desire for quality and implement the best approach to a client situation/scenario to ensure correct analysis without an over complex process

GVR BIO SCINCE offers clinical data management services that are specialized; clinical research organizations can stand to ensure that the quality of data is superior and also offers an assurance as to the integrity of the clinical data.

GVR BIO SCIENCE offers clinical data management services that are specialized; clinical research organizations can stand to ensure that the quality of data is superior and also offers an assurance as to the integrity of the clinical data. GVR BIO SCIENCE assures that the data that is being managed totally and absolutely complies with international standards with a view to ensure consistency within clinical data.

GVR BIO SCIENCE offers the following services:

Clinical data management is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials.

  • Developing CRF /eCRF papers.
  • Double-key data entry.
  • Data validation.
  • Query generation & resolution.
  • SAS datasets.
  • Clinical data management process and is normally mandated by SOP.
  • supervises the CDM process
  • codes variations such as adverse events and medical history
  • hecks the accuracy of data entry and performs data audits
  • racks the receipt of CRF pages and enters data into a database
  • CRF printing and distribution
  • design and set up of the clinical database.
  • Ascribes to the specifications as laid down by CDISC CRT-DD.
  • Before and after marketing clinical studies.
  • Adherence to Clinical Data Interchange Standards Consortium (CDISC)