A document management software is an automation tool to manage every step of the document lifecycle, right from its creation to publishing and storing.

EU MDR (The European Union Medical Device Regulation) is a regulatory framework applies to all medical device manufacturers and distributors intended to improve the safety of healthcare and the performance of medical devices in Europe.

Hazard analysis is the process of identifying hazards that have the potential to arise from a system or environment, documenting their unwanted consequences, and analyzing their underlying causes.

CAPA FDA is a quality management strategy used in the manufacturing and production industries to meet the intent of the FDA 21 CFR 820.100 requirements. This guide explains why, how and instructions to achieve the ten objectives of CAPA FDA.

What is Risk Management? Risk management comprises the identification, analysis, and response to risk factors attempting to control future outcomes by acting proactively rather than reactively.

Risk mitigation is a systematic process where an organization develops actions and options to increase opportunities and reduce threats to project objectives.

A webinar by ComplianceQuest on safety and health technology trends to watch in the 2020s. Learn about workplace safety and employee well-being.

This webinar about complaints management is presented by Deb Kacera with over 20 years’ experience in quality, post-market complaints, risk and compliance in the medical device and manufacturing industries.

Watch webinar and gain key information related to FDA’s response to COVID-19 pandemic. Learn what the FDA looks for in the crucial risk-benefit section.

Digital transformation in quality management for life sciences and manufacturing industries, offers a continuous optimization of the complete quality cycle for maximum value.

A strong working relationship between suppliers and manufacturers not only delivers cost savings, it also minimizes inventory availability problems, production and shipping delays, as well as quality and safety issues.

Watch CQ video and explore how companies are managing their suppliers and what they are doing to better reap its rewards across the lifecycle of a supplier.

Watch CQ webinar on understanding the 2021 regulatory expectation for data and metadata integrity providing detailed instructions.

Watch ComplianceQuest webinar on the EHS transformation journey for safety culture and operation excellence.

Watch CQ video and explore how artificial intelligence and machine learning will be among the top innovations this decade in medical technology.

Watch ComplianceQuest webinar and explore how next gen techniques to design and develop innovative medical technology.

In this whitepaper, we share our expertise about the finer nuances of supply chain management from a quality perspective.