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Request Information - Novatek International News Updates - 1 CFR Part 11 Compliant - Out-of-the-box LIMS software solutions

Novatek Medical Data Systems
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SOLUTIONS » Specialty products » Clinical Assay Management Software (CAMS)©

Clinical Assay Management Software (CAMS)©
Novatek’s Clinical Assay Management LIMS software solution (NOVA-CAMS) facilitates best practice business processes for clinical sample tracking, clinical analytical data request and receipt, quality control and quality assurance. It provides a consistent approach for managing all analyses across the study and ensures a single, verifiable version for all clinical analytical data.

Novatek Clinical Assay Management LIMS software (NOVA-CAMS) uses a flexible workflow to allow structured validation, quality assurance (QA), signoff and distribution of data. QA is built into the workflows to ensure it is reviewed as data are receipted allowing initiation of immediate corrective measures.
The Novatek Clinical Assay Management LIMS software (NOVA-CAMS) solution is designed to meet current regulatory and audit requirements by tracking every data change and requiring appropriate authentication to undertake any activity within the system.

The solution includes sample and result registers, sample dispatch, compliant results receipt and distribution.


Planning assay and dilutions for each sample type

The Novatek Clinical Assay Management LIMS software solution:

  • Plate Management System
  • Tray Management System
  • Streamlines the clinical assay management process.
  • Reduces regulatory compliance costs by providing systematic and auditable processes for handling clinical data.
  • Allows centralization of clinical data management functions without loss of functionality, reducing costs, enabling greater organizational flexibility and securing critical data.
  • Facilitates analysis of clinical data, enabling early problem detection and resolution. Novatek clinical LIMS integrates with other Novatek products providing streamlined analytical data.

There is a large Risk associated with assay data especially those of clinical data. Assessing and managing risk, as well as establishing areas of uncertainty which contribute to risk, are critical to a company’s decision making processes. The Novatek Clinical Assay Management LIMS software (NOVA-CAMS) enables those involved in Clinical assay process to understand the nature and interdependence of risk in the business process. NOVA-CAMS goes beyond conventional clinical assay quality management processes, by evaluating integrated internal and external assay information, hosted within transparent and auditable databases.



Clinical Assay Management solution| Clinical Trials Software
Novatek International News Updates - 1 CFR Part 11 Compliant - Out-of-the-box LIMS software solutions
APP Pharmaceuticals Goes Live with Novatek's Environmental Monitoring LIMS Software (NO-VA-EM). APP Pharmaceuticals chose Novatek International for automating its environmental monitoring processes at multiple locations within the USA and as of the beginning of this month, went live with the Nova-EM software.

Feb, 2010
APP Pharmaceuticals Goes Live with Novatek's Environmental Monitoring LIMS Software (NO-VA-EM). ....

Dec, 2009
Montreal, Canada, Dec, 2009.
Novatek International, the pioneer of 21 CFR Part 11 compliant LIMS would like to announce that Solumed a subsidiary of 3M ...

Sept, 2009
Pyramid Labs, CA, USA and Novatek.
Novatek International, the pioneer of 21 CFR Part 11 compliant LIMS would like to announce that Pyramid Laboratories, CA, USA has chosen ...

July, 2009
JHP Pharmaceuticals and Novatek
JHP Pharmaceuticals choose Novatek International for automating their Environmental Monitoring and Quality System management processes ...

July, 2009
Medtronics, MN, USA and Novatek.
Novatek International, the pioneer of 21 CFR Part 11 compliant LIMS would like to announce that Medtronics, MN has chosen Novatek’s Stability LIMS software solution ...

Novatek International Events Updates - 1 CFR Part 11 Compliant - Out-of-the-box LIMS software solutions
Drug Master Files (DMFs)
Strategy for Meeting Your Regulatory and Processing Responsibilities February 23-24, 2010 - Jersey City, USA
4th Pharmaceutical & Biotech GMP Conference
Ensuring Patient Safety through Good Manufacturing Practices February 21-23, 2010 | Dubai, United Arab Emirates
Fundamental Tools in Statistics for GMP Compliance
A Two-Day Case Studies & Workshops for Life Sciences Professionals February 2-3, 2010 - Greater New York city Area, USA.
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