• Bringing revolution of automation in the world of Clinical Trial

     
  • Ideal for small, mid or large cap CROs & Pharma Sponsors, Hospital involved in Clinical Research

  • 21 CFR Part 11 Compliant Validated & Certified by independent Consulting Agency Server & Cloud Based Option

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About Us & What We Do

Bioquick is a full fledge EDC solution developed on basis of several guidelines of Clinical Research to ensure that the data collected during the various processes are captured directly through the electronic Software for better compliance, transparency and integrity.

Volunteer/Patient Database

With the time Clinical Research is one of the attraction for several people in market to become a participant of the Clinical Study.

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Medical Screening

For a Phase-I/BA-BE study Medical Screening is a unique visit where the volunteer is checked for the fitness by undergoing various Medical tests.

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Study Set Up

With every protocol the design of the study is different. Without programming skills anyone can design compliant clinical studies...

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Data Collection

Once the Study is Set Up and deployed, Clinical operators can start capturing the data as per the CRF. However, there is more than...

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Data Capture

Once the Study is Set Up and deployed, Clinical operators can start capturing the data as per the CRF. However, there is more than...

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Data Export/Import

Bioquick provides the data extraction into variety of the formats as per the need of the Clinical Trials It can be exported...

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Project Management

Bioquick provides an intensive tool to help the project managers in tracking the projects to ensure timely delivery. It gives an...

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Sample Management

Samples are the most important for the analysis of the Clinical Study. The entire status of the study depends on the collected samples.

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