top of page
242370_d4ad4c2b4cb64078b983797d23c92274~

QMexCOPAN SaaS Takes the Time Allocated for Quality Management and Technical File Document Preparation Processes and Gifts It to You

Request a Demo

Designed to Support Medical Device Manufacturers

Quality management in the medical device industry is vital for the safety of patients and the performance of products. QMexCOPAN , developed in cooperation with EXCOPAN and BTS , is an innovative quality management system that allows you to manage all quality management processes on a single platform.

QMS Redefined

QMexCOPAN is a software that facilitates compliance with legal requirements, designed modularly for the purpose of operating quality processes electronically, integrated with each other and with other business applications, complying with the requirements of 21 CFR Part 11 and can be used through internet browsers validated according to GAMP 5.

Cost Advantage

Time and human resources, paper, printing materials, physical archive.

Data Integrity

Secure data storage and monitoring in compliance with ALCOA+ requirements.

Easy Reporting

Easy reporting with PDF, Excel and Dashboard features.

Saving time

Monitoring whether actions are carried out correctly and on time, ease of auditing, fast document preparation, approval and distribution.

Data security

Customer-specific, isolated on the MS Azure SaaS platform;

  • Database

  • Storage Services

  • App Services

Full Compliance with Regulations

It is designed to be 100% compliant with international regulations such as ISO 13485, FDA QSR, MDR, IVDR. Thanks to instant update capabilities, you can instantly integrate changes in legislation into the system.

QMexCOPAN's Functions That Make Your Life Easier

  • Electronic signature

  • System and module based authorization

  • LDAP integration

  • Audit Trail

  • Registration history

  • Action-based and scheduled notifications

  • Personal Page: Pending Tasks, Delegated Tasks, Bookmarks

  • dashboard

  • Graphic reports

  • Trend reports

  • Validated reports

  • Printer-friendly versions of records

  • Configuration screens

  • Adding multiple files

  • Related Records screen, which allows you to view records related to each other

  • Multiple location support

  • Multi-language support

  • Different reporting and sorting options

  • Inter-module integration

  • Ability to integrate with all 3rd party software, including ERPs

  • Powerful workflow management

  • User-friendly interfaces

Contact Us to Request a Demo and for Information

WhatsApp_Image_2024-02-06_at_13.24_edited.png

+90 532 221 4500

enstitu@saglik.org.tr

Anıttepe, 06000 Çankaya/Ankara

Stay Informed about the Latest Developments

Follow us:

  • LinkedIn
  • Facebook
  • Twitter

© 2024 Medical Devices Institute.

bottom of page