Orcanos Blog

Summus Laser Selects Orcanos to Revolutionize Quality Management in the Laser Therapy Market
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October 29, 2024
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4
min read

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

Rami Azulay
Rami Azulay
Founder & CMO
News
QMS Software for Medical Devices
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March 5, 2024
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8
min read

QMS Software for Medical Devices

News
Empowering Your Quality Management with AI-Driven Automation
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October 11, 2023
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11
min read

Empowering Your Quality Management with AI-Driven Automation

Best Practices
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
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July 8, 2023
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34
min read

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

Compliance

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Technology
How to Succeed in the Automotive Industry?
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January 19, 2020
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6
min read

How to Succeed in the Automotive Industry?

Best Practices
10 Tips To Ensure Your GMP is a Quality Priority
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July 29, 2019
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34
min read

10 Tips To Ensure Your GMP is a Quality Priority

Tips
CAPA: Corrective and Preventive Actions Introduction Principles – Chapter I
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July 7, 2019
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23
min read

CAPA: Corrective and Preventive Actions Introduction Principles – Chapter I

Compliance
cGMP – Design Inputs (URS-FRS-MRS-ERS) – ISO 13485:2016 (7) Clause 7
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May 30, 2019
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12
min read

cGMP – Design Inputs (URS-FRS-MRS-ERS) – ISO 13485:2016 (7) Clause 7

Compliance
Risk Management (03) – The Regulatory Requirements For Risk Management
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May 12, 2019
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13
min read

Risk Management (03) – The Regulatory Requirements For Risk Management

Compliance
cGMP – Design & Development Plan (DDP) – ISO 13485:2016(6) Clause 7
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May 11, 2019
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9
min read

cGMP – Design & Development Plan (DDP) – ISO 13485:2016(6) Clause 7

Compliance
cGMP – Customer Related Processes and Requirements – ISO 13485:2016(4) Clauses 7
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May 4, 2019
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13
min read

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

Compliance
Current Good Manufacturing Practice (cGMP) and ISO 13485:2016 – Validation Master Plan (VMP)
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April 18, 2019
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25
min read

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

Best Practices
Orcanos e-QMS 4.0 – The new MRB process, getting it all in one place, how it works!?
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November 10, 2018
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7
min read

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

Best Practices
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