Audience
Bio-Medical companies (including Biotech, Pharma and Medical Device)
About Qualcy QMS
Qualcy Bio-Med QMS Software has been designed for Bio-Medical companies (including Biotech, Pharma and Medical Device) to manage QMS records for ISO13485 and FDA requirements. * Designed for meeting the requirements for 21 CFR Part 820 * Has built in features for E-sign, audit trails and complies with 21 CFR part 11 requirements. This software helps manage the records for Doc. change control, complaints, audits, CAPA, NC Records, Training Records and more.
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Product Details
Qualcy QMS Frequently Asked Questions
Qualcy QMS Product Features
Calibration Management
Quality Management
Qualcy QMS Additional Categories
Qualcy QMS Verified User Reviews
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"Good QMS software" Posted 2021-02-24
Pros: Simple and easy to manage the document change controls. Integrated training module automates the training records. The QMS package comes with calibration and asset management module, which is a big plus.
Cons: It took us little longer than expected to get started. It has been a good experience so far.
Overall: Good software for biotech companies. The built in compliance and part 11 features are big help. Good support from the Qualcy team.
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