Accelerating Medical Device Development with Jama Connect

Jama Software

Jama Connect for Medical Device Development

In this post, we’ll explore how Jama Connect for Medical Device Development is designed to help you get ramped up quickly with a platform, training, and documentation aligned to industry regulations ISO 13485:2016, 21 CFR 820.30, and ISO 14971:2019, while applying a proven systems engineering approach to product development.

With this solution, medical device teams can manage design controls for device requirements and related risks, simplifying regulatory submissions and audit preparations while accelerating time to market.

Manage Design Controls for Device Requirements and Related Risks in a Single Platform

Easily Demonstrate Traceability

Traceability ensures that design inputs have been met and verified, providing necessary evidence from the design control process. Jama Connect allows you to easily produce traceability documentation required by regulators.

Manage Risk Analysis

Manage risk analysis, aligned with ISO 14971:2019. Jama Connect helps teams identify and mitigate risks earlier in medical device development, saving teams from frustrating late-stage design changes and supporting the path to regulatory compliance.

Maintain Audit Trails and Export Data

Real-time reporting and baselining allows you to track all changes to information within the system, including timestamps and associated users. Data is easily exported from Jama Connect if your current process dictates storage of documentation in a quality management system (QMS).

Reuse and Baseline Management

Compare versions of a requirement, generate branches to develop a variant, and create catalogs of reusable requirements to improve medical device development.

Compliant Reviews and Approvals

Increase early stakeholder visibility and participation in the review process with electronic signatures that are compliant with FDA 21 CFR Part 11.

Design Verification and Validation

Seamlessly manage traceability to verifications and validations, providing evidence to comply with government regulations and standards, like 21 CFR Part 820.30.

Flexible, Scalable Options with Jama Connect for Medical Device Development

Jama Connect for Medical Device Development Solution’s license model is fully scalable, ensuring rapid deployment and easy adoption of the solution across your product development team. It also allows flexibility and can be customized to your team’s unique needs. Download this datasheet to learn more about key product benefits and features, unique licensing types, and templates templates provided as part of the solution.

To see more information specific to the medical device development industry, we’ve compiled a handy list of valuable resources for you!


Previous Article
What Is Product Development Lifecycle Management?
What Is Product Development Lifecycle Management?

In this blog, we answer the commonly asked question, "what is product development lifecycle management" and...

Next Flipbook
Accelerate Innovation in Medical Device Development
Accelerate Innovation in Medical Device Development

In this infographic, you’ll learn how Jama Connect can help accelerate innovation, maintain product quality...