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Process Automation Software In Singapore
4 software items found
by:Novatek International based inMontreal, QUEBEC (CANADA)
All healthcare and life science organizations that develop and manufacture products rely greatly on accurate informative text and printed labels to communicate to their end user and build their product brands successfully. Novatek’s software provides effective proof reading results to support the industry’s highest standards; eliminating printing errors in all product information ...
by:MasterControl, Inc based inSalt Lake City, UTAH (USA)
Small Medical Device Companies Can Now Manage and Automate their Design Control Process to Ensure Compliance with 21 CFR Part 820 with the Help of MasterControl's Design Control Software Systems at a Low Monthly Cost. Each manufactured medical device must be supported by appropriate documentation which demonstrates that its development followed the Food and Drug ...
by:MasterControl, Inc based inSalt Lake City, UTAH (USA)
OOS Software to Automate Out of Specification (OOS) Processes to Comply with FDA CGMPs and 21 CFR Part 211 and Part 820 Regulations. In the FDA environment, specifications are essential in maintaining quality. CGMP regulations for finished pharmaceuticals (21 CFR Parts 210-211) and medical devices (21 CFR Part 820) require strict conformance to approved ...
Manufactured by:Particle Measuring Systems (PMS) based inBoulder, COLORADO (USA)
The top Data Collection and leading Data Management companies combined to create a complete contamination monitoring solution for pharmaceutical manufacturers. Plus, with its unique plug and play ability, portable devices and monitoring, system connection has never been ...