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5 Ways MasterControl Ensures System Compliance With 21 CFR Part 11

2013-09-05 03:32:38| drugdiscoveryonline Downloads

Under 21 CFR Part 11, FDA-regulated companies that choose to maintain electronic records to meet predicaterules are required to validate their electronic record-keeping systems.

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MasterControl Clinical Suite Brochure

2013-08-28 07:42:09| drugdiscoveryonline Home Page

The management of clinical trials is one of the most costly and time consuming processes in the development of a typical product.

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MasterControl Pharma R&D Brochure

2013-08-28 07:25:08| drugdiscoveryonline Home Page

Even a single day’s delay in getting a product to market can result in the loss of millions of dollars of potential profits. MasterControl Pharma R&D is a utopian software solution that integrates advanced document management with a training component to create an unparalleled system specifically preconfigured for pharmaceutical companies’ document and project management needs.

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MasterControl GCPDocs JumpStart Brochure

2013-08-28 07:15:06| drugdiscoveryonline Home Page

For many years, the conducting of clinical trials relied on the integrity of the personnel involved in operating the trial. The introduction of good clinical practice (GCP) principles established an era of regulation previously unknown in the pharmaceutical and biotechnology industries.

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MasterControl TotalPharma Brochure

2013-08-28 07:00:20| drugdiscoveryonline Home Page

Managing documents, training, and business processes are nightmares shared by all pharmaceutical and biotech companies. MasterControl TotalPharma™ exchanges the nightmares for a dream of a solution that enables these companies to get their products to market faster and improve compliance at the same time.

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