CAQ AG Factory Systems
Menü Suche
Quality Excellence in Medical Technology
ISO, FDA, MDR: Discover the Software for Consistent Compliance with Standards

Medical Technology Webinar (held in German)

Today more than ever, medical technology companies need to take advantage of the benefits of digitization and incorporate these into their daily processes in order to ensure increased patient safety, competitiveness, and compliance with standards. Learn in our 60-minute webinar on June 4, 2020, how CAQ.Net software solutions simplify the fulfilment of quality-related guidelines such as ISO 13485, MDR, or FDA 21 CFR 820. The webinar is free of charge and will be held in German.

Risk analysis in accordance with ISO 14971

Quality assurance in medical technology is in a constant state of change, which is not least characterized by ever new demands on manufacturing companies. Especially in the last few years, the revision of ISO 9001 and ISO 13485 as well as the introduction of the new MDR (Medical Device Regulation) have created several stricter regulations which must be observed.

Comply with Standards, Laws, and Regulations

Our CAQ.Net® software was developed precisely to support companies in the structured implementation of standards, laws, and regulations. Learn from our experts in our webinar on June 4, 2020 at 2:00 p.m., how CAQ.Net® ensures consistent compliance with the most important quality management standards from field of medical technology. Among other things, the digital implementation of the following topics will be explained:

1. Documents

How to practice successful document management in compliance with ISO 13485:2016 4.2.4 / 4.2.5 and FDA 21 CFR 820.40 with our QBD.Net module

2. Trainings

How our Qualify.Net module supports you in implementing a holistic training and qualification management system in accordance with ISO 13485:2016 6.2 and FDA 21 CFR 820.25

3. Risks

How you can achieve an ISO 1497 compliant application of risk management using our Risk.Net module

4. Complaints / CAPAs

How to master Corrective and Preventive Actions in terms of FDA 21 CFR 820.100 and ISO 13485:2016 8.2.2, 8.5.2 / 8.5.3 with our REM.Net module

Users from Within the World of Medical Technology Report

Find out in our case studies how leading companies in the medical technology industry use our software solutions to raise the quality of their products to world-class levels and continuously improve themselves. Read:


Additional Links
This website uses cookies for an improved user experience. For more information regarding cookies, please consult our data privacy policy. OK