Orcanos Blog

Summus Laser Selects Orcanos to Revolutionize Quality Management in the Laser Therapy Market

October 29, 2024

Summus Laser Selects Orcanos to Revolutionize Quality Management in the Laser Therapy Market

Rami Azulay

Best QMS Software for Medical Devices: A Review of Orcanos

Best QMS Software for Medical Devices: A Review of Orcanos

Empowering Your Quality Management with AI-Driven Automation

October 11, 2023

Empowering Your Quality Management with AI-Driven Automation

Top 10 questions you need to ask any eQMS vendor for ensuring Regulatory Compliance: ISO13485, FDA 21 CFR Part 820, and 21 CFR Part 11

Top 10 questions you need to ask any eQMS vendor for ensuring Regulatory Compliance: ISO13485, FDA 21 CFR Part 820, and 21 CFR Part 11

Latest Articles

cGMP – Customer Related Processes and Requirements – ISO 13485:2016(4) Clauses 7

cGMP – Customer Related Processes and Requirements – ISO 13485:2016(4) Clauses 7

Current Good Manufacturing Practice (cGMP) and ISO 13485:2016 – Validation Master Plan (VMP)

Current Good Manufacturing Practice (cGMP) and ISO 13485:2016 – Validation Master Plan (VMP)

Orcanos e-QMS 4.0 – The new MRB process, getting it all in one place, how it works!?

November 10, 2018

Orcanos e-QMS 4.0 – The new MRB process, getting it all in one place, how it works!?

How To Measure Your Software Maturity Performance

How To Measure Your Software Maturity Performance

FDA approves a framework similar to Orcanos that simplifies the CAPA process for medical device manufacturers, making it easier to implement.

FDA approves a framework similar to Orcanos that simplifies the CAPA process for medical device manufacturers, making it easier to implement.

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