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MasterControl Audit Brochure

2013-08-28 05:16:20| drugdiscoveryonline Home Page

A quality audit is to a regulated company what a medical examination is to a patient. It is a necessary and repeating procedure for evaluating a quality system’s general “health” and for “diagnosing” problems in order to correct them. In the FDA and ISO environments, quality audits are required on an ongoing basis to help improve product quality and safety — and to ensure compliance.

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MasterControl Clinical Lab JumpStart Brochure

2013-08-28 04:35:53| drugdiscoveryonline Home Page

The detailed documentation needed to meet CAP and ISO 15189 requirements could conceivably require organization and storage of thousands of pages of procedures, policies, and work instructions.

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MasterControl Training Brochure

2013-08-28 04:25:22| drugdiscoveryonline Home Page

In regulated industries, such as the FDA and ISO environments, companies are required to implement and document employee training to ensure that their personnel know how to perform their duties within company and industry guidelines.

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