Change control management is a systematic technique to ensure that a change does not negatively impact a product’s safety, quality or compliance. Change management solution is an essential part of any project or product management.

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21 CFR part 11 is Part 11 of Title 21 of the Code of Federal Regulations by FDA as compliance guidelines for trustworthiness of electronic records and electronic signatures.

Supplier Management Software is a cloud-based software to manage the complete supplier lifecycle and supply chain management across all locations.

Cost of quality or COQ is defined as estimation for prevention, detection and elimination of defects to improve product quality.

These 4 ways will definitly help you minimizing non conformance there by helping you to improve the quality

CAPA management software enables you to identify and investigate non-conformance and discrepancies caused in a system for a faster rectification of problem.

FDA design control is defined as an interrelated set of quality practices and processes for medical devices design and manufacturing.

Audit management software system designed to manage your end-to-end process in a faster and effective way to increase your productivity by decreasing manual documentation.

Quality Management System or QMS software evaluates the set of policies, processes, and procedures of a company for complex product development in various highly regulated industries.

An environmental management system software is a strategic framework which helps in tracking, managing and reporting environmental performances to comply with government regulations.

Design control is a part of the comprehensive quality standard set by the FDA to assure medical device manufacturing is risk-free for users and patients.