Deliver compliant, high quality products faster.

Integrate quality into your development process with a scalable software platform that helps reduce regulatory burden while empowering team collaboration throughout the product lifecycle.

Trusted by 200+ SxMD & Medical Device Companies

Navigate quality processes effectively

Redefine quality and compliance by integrating your systems for complete visibility. Make it easier to plan and prepare your QMS and product documentation for audits.

Streamline document management

Efficiently review, approve, update, and link documentation. Generate accurate documents with part 11 compliant eSignatures in the format you need to make your next audit painless.

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Matrix ALM
Digitally track and manage Quality

Keep go-to-market plans on track with the right implementation procedures by managing CAPAs, audits, feedback and the review and approval process in one centralized place.

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Achieve training compliance

Acquire valuable insights into quality events and coordinate training or retraining workflows on procedures proactively to mitigate errors before they impact your go-to-market plans. 

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Real-time audit readiness

Visual traceability between your design and quality systems provides teams with the information they need throughout the entire process to easily identify missing or suspect data to ensure audit.

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Standardize with pre-defined templates

Simplify reporting and document control with pre-defined and customizable templates that can be created, updated and shared with select projects.

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Hear from our customers


“We’ve cut the number of FTEs working on document control tasks by 50%, which frees our employees to focus on value-added activities.”

Umesh Sharma, Head QA/RA, Meril Life Sciences