Building Your BOM: 3 Ways To Manage Your Product Information With Full Traceability

FREE ON-DEMAND WEBINAR

Building Your BOM: 3 Ways to Manage Your Product Information with Full Traceability

Too often medical device product development teams rely on manual processes or disconnected solutions to manage evolving product designs and data.

These ultimately create data silos and room for error that can bear the risk of increased costs, compliance risk, and submission or production delays. Turning a team’s focus from innovative design to cumbersome paperwork and information management.

Now, with Greenlight Guru Products, you gain more control of continuous product development, connected to their device history file (DHF) and quality actions—all in one place.

Create a seamless flow from product development processes to DHF and manage critical components of your device master record (DMR) while achieving traceability throughout the total product lifecycle.

Watch the webinar

Specifically, this webinar will cover:

How to overcome data silos and reduce the risk of communication gaps and common errors that increase costs, and delays during product development
How to build and manage your items and multi-level bills of materials (BOMs) while you design your medical devices
Proven strategies for streamlining engineering change and building traceability throughout the entire device lifecycle.
Capabilities of Medical Device Product Management within a Medical Device Success Platform
Q&A session

Who Should Attend?

Product Development Engineers and Management
R&D Engineers and Management
Quality Professionals and Management
Medical Device Executives

Hosted by

Presenter: Alex Butler

Senior Product Manager, Greenlight Guru

Moderator: Jesseca Lyons

Operations and Enablement Guru, Greenlight Guru

About Greenlight Guru

Greenlight Guru is the only quality management software platform designed specifically for medical device companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.

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Featured Capabilities: