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$14M to Build the Future of Medical Software

Erez Kaminski
  •  
December 4, 2023
December 5, 2023
On December 5, 2023, Ketryx announced its Series A funding of $14 million led by Lightspeed Venture Partners with participation from existing investors E14 Fund and Ubiquity Ventures. Company CEO & Founder Erez Kaminski reflects on how we got here and what the investment means for better, safer software—and more of it.
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Product Announcements

Announcing Ketryx’s UL Certification to IEC 62304, ISO 13485, and ISO 14971

Paul Jones
  •  
April 19, 2024

Ketryx 2.6

Erez Kaminski
  •  
April 9, 2024
March 29, 2024
FDA

21 CFR Part 11 Compliance Guide for Jira (Atlassian)

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  •  
March 19, 2024

Ketryx 2.5

Erez Kaminski
  •  
March 30, 2024
February 13, 2024
AI/ML

MedTech Trends for 2024: Takeaways from JP Morgan's Health Conference

Erez Kaminski
  •  
January 25, 2024
January 25, 2024

$14M to Build the Future of Medical Software

Erez Kaminski
  •  
January 10, 2024
December 5, 2023
Traceability

IEC 62304 & Requirements Traceability Matrix (RTM) in Jira: A Guide for Medical Device Companies

Jan Pöschko
  •  
March 30, 2024
AI/ML

How to generate an SBOM (Software Bill of Materials) fast

Jan Pöschko
  •  
March 30, 2024
November 2, 2023
Regulations

Ketryx Guide to RAPS Convergence 2023

Bailey Pearlman
  •  
October 3, 2023

The latest (June 2023) changes to the FDA’s new premarket submission guidance

Lee Chickering
  •  
December 4, 2023
October 16, 2023
Regulations

Ketryx’s guide to DTxEast 2023

Bailey Pearlman
  •  
October 3, 2023
September 14, 2023
FDA

Simplifying 510K Submissions with FDA’s eSTAR Program and Ketryx

Paul Jones
  •  
October 20, 2023
September 12, 2023

Best Practices for Maintaining a Requirement Traceability Matrix in Agile

Jake Stowe
  •  
September 6, 2023
Regulations

PATCH Act: How to Comply in 2023 & Beyond

John Koontz
  •  
December 4, 2023
August 16, 2023
Traceability

The Best RTM Tools for Agile Teams: Looking Beyond Excel

Jake Stowe
  •  
March 30, 2024
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2023 FDA Warning Letters and Software Validation

Erez Kaminski
  •  
August 30, 2023
August 9, 2023
Regulations

Clinical Trial Computerized Systems Regulation Review

Jake Stowe
  •  
December 4, 2023
August 9, 2023
Traceability

The Ultimate Guide to Requirements Traceability Matrix (RTM)

Jake Stowe
  •  
March 30, 2024
June 19, 2023
Traceability

Ketryx 2.0 Release

Erez Kaminski
  •  
December 4, 2023
May 11, 2023
Regulations

The FDA drops a Cybersecurity Compliance SBOM in 2023

Erez Kaminski
  •  
December 4, 2023
July 19, 2023
Regulations

The Turtle Problem

Jake Stowe
  •  
December 4, 2023
April 13, 2023
Regulations

Why the FDA’s Most Common Warning Letter Might Surprise You

Erez Kaminski
  •  
August 30, 2023
August 24, 2023
Regulations

Key Takeaways from the first Safety-critical Software Meetup in Boston

Erez Kaminski
  •  
August 30, 2023
April 13, 2023
Traceability

A brief overview of cloud security for standard and safety-critical software

John Koontz
  •  
August 30, 2023
April 17, 2023
Regulations

Computer Software Assurance

John Koontz
  •  
March 30, 2024
April 17, 2023
Regulations

SOUP Software Definition and a Guide to Software Regulations of Unknown Provenance

Erez Kaminski
  •  
December 4, 2023
May 12, 2023
AI/ML

Creating FDA-compliant Medical Devices at Lightning Speed with ChatGPT and Ketryx

Felipe Asfura
  •  
August 30, 2023
April 13, 2023
Regulations

FDA Traceability Matrix Requirements for Medical Devices

Jake Stowe
  •  
February 29, 2024
May 26, 2023
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