Qaira.io

12/11/2019

Meet us in Medica! https://www.medica-tradefair.com/

QAiRA ( Qaira.io ) is a cloud based SaaS for Medical Device -sector for monitoring regulations, tracking regulatory requirements and complying to the requirements. The service was created by medical device professionals from Kasve Oy

https://www.kasve.fi/en/meet-qaira-and-kasve-in-medica/

QAiRA and Kasve are joining Medica! Our goal is to introduce the QAiRA cloud service and collect feedback, views and opinions about the service.

06/09/2019

Kasve Oy has become the 100% owner of Qaira Ltd and as a result, operations of Qaira Ltd were merged into Kasve Ltd. Now QAiRA’s story continues as product of Kasve Ltd, and thanks to this change, the expertise of Kasve´s QA and RA experts can be used more effectively in QAiRA’s development.

More information:

Kasve Ltd became the 100% owner of Qaira Ltd and as a result, operations of Qaira Ltd were merged into Kasve Ltd. Now QAiRA's story continues as product of Kasve Ltd, and thanks to this change, the expertise of Kasve´s QA and RA experts can be used more effectively in QAiRA's development.

22/08/2019

New service, the Qaira News Portal is available for companies from the beginning of August 2019. The main goal is to provide …

14/05/2019

QAiRA - Comprehensive Online Toolkit for Medical Device Regulatory Management:

- Always up-to-date regulation, guidance and standards
- Easy-to-use checklists for technical documentation and QMS
- Online product management with regulatory overview

To check out the key features of QAiRA, please visit www.qaira.io

13/05/2019

Two more days to go!

What is QAiRA? 👉 www.qaira.io

Information in Finnish:
https://www.kasve.fi/qaira-palvelun-julkaisu/

19 followers

08/05/2019

Qaira Ltd is a software company founded by medical device and software professionals. QAiRA -service was created out of organic need to follow regulatory requirements digitally and automatically. This is crucial from Medical Device Regulation (MDR) viewpoint, because medical device manufacturer needs to follow and show evidence that applicable regulations and standards are followed. The service is currently in piloting phase and target for release is in early autumn 2019.

For additional information please visit www.qaira.io or contact [email protected]

QAiRA helps medical device manufacturers to easily manage and track their own products' regulations and standards and keep them updated. QAiRA covers the European medical device regulations at launch, global regulations in the near future.