AQA Company develops quality management software designed specifically for medical device companies. The software complies with US, Canadian and Australian regulations. It is formally validated to FDA, ISO and IEC requirements and complies with 21 CFR Part 11(Electronic Records and Electronic Signatures). We have added 4 new modules, Automated Training, Preventive Maintenance, Change Control and Risk Management module. The Training module will automatically generate and post new/revised document training courses. Automatically generate and post of other training courses (self-study, class and job training). Assign and schedule employees/groups to document training and other training programs. The Preventive Maintenance module has spare parts inventory management and will automatically generate maintenance work orders. The Risk Management module has two different ways to to calculate risk, you choose which is best suite for your device.
Avetta connects the world's leading organizations with qualified suppliers, contractors and vendors. Our supply chain management solution removes your administrative overhead and reduces your cost of qualifying, managing, and monitoring contractors and suppliers.
All over the world, in... Read More
RJ Lee Group is an industrial forensics analytical laboratory and scientific consulting firm located in the Greater Pittsburgh area. We partner with our clients to deal with problems encountered during the manufacturing process, to ensure regulatory compliance, and to uncover and understand the... Read More
CloudApper is a SaaS solution platform empowering businesses to automate tasks, improve productivity, and augment IT resources.
CloudApper enables anyone to easily create the apps they need to unleash the true power of their devices. It’s an intutive platform that businesses and individuals can...
