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Labcompliance News, February 2000

February 24, 2000

EU GMP Draft Validation Master Plan

Validation master plans are not specifically required by the FDA. However, the FDA wants to know your approach towards validation. A master plan is the ideal tool. You can get a free Equipment Validation Master Plan when you join the Labcompliance Userclub. The master plan is both concise and comprehensive. Whether you use it as it is or as a template: it saves time and increases confidence for inspections.
for more information click here

February 14, 2000

ISO/IEC Guide 25 revised to ISO 17025


The ISO/IEC Guide, "General requirements for the competence of calibration and testing laboratories", has been revised and is expected to be issued as ISO/IEC Standard 17025 in February 2000. Affected laboratories will be required to the new standard within two years from the date of publication of the standard. Until it's final release you still can download the draft version ISO/IEC DIS 17025 from the Internet. .