Evolving to MedDev 2021

April 27 - 29, 2021 | Online

Evolving to MedDev Recorded Sessions

Welcome Session and Bridging the Gap from Aerospace Manufacturing to Medical Device Compliance

After a brief introduction about the inaugural Evolving to MedDev 2021 event, learn how aerospace manufacturers can begin their journey to FDA Medical Device compliance & approval.

Applied Explainable AI in Manufacturing

Learn the importance of Explainable AI, the implementation challenges, & where theory & practice diverge in implementing explainable solutions for manufacturing.

Case study: University Minnesota's Collaboration with Ford to make Air Filtration Devices

Learn how Ford and UMN teamed to develop air filtration kits people can make at home or in school to help reduce COVID-19 virus particle concentrations.

An Introduction to MedAccred and MedAccred Suppliers Panel

Quickly gain an understanding about MedAccred certification criteria and hear from medical device manufacturing suppliers who discuss achieving MedAccred Accreditation and how it has strengthened their business within the medical device industry.

Panel: Pivoting to MedDev

Experts from Barnes Global Advisors, along with Martin Petrak, CEO of Precision ADM, discuss practical considerations necessary for a pivot to medical devices.

Miniaturization in Manufacturing

Hear how Boston Micro Fabrication is enabling miniaturization and why manufacturability is no longer the limiting factor in product design.

Additive Manufacturing for Aerospace

Learn how additive manufacturing lends itself to replace conventionally manufactured parts and assemblies with lightweight components for aircrafts and engines.

Improve Public Health by Utilizing Existing Expertise in the Aerospace Industry

Uncover opportunities to improve public health by utilizing expertise in the aerospace industry, which is surprisingly aligned with the medical devices industry.

Why Get into Medical Devices and How Might You Do It

A primer about the medical devices industry covering expansion possibilities, regulations, certifications, and the best places to enter into the market.

America Makes: Its Pivot to Medical and Rules of Engagement to Transition

America Makes discusses its pivot from aero to medical to support the US’s COVID mitigation plan, and the rules of engagement for AM that apply to many sectors.

Opportunities and Challenges in MedTech & Robotic Surgery

Companies interested in entering MedTech will receive practical advice from FUTEK on topics such as safety, efficacy, regulation and finding industry partners.

Building a Diverse, STEM-Fluent Workforce with the SAE Foundation

Learn how the SAE Foundation can help you achieve your CSR and STEM outreach goals with SAE’s hands-on STEM education programs in your target communities.

Medical Device Quality Management System Requirements and the Value of ISO 13485 Certification

Understand the value of ISO 13485 certification, “commercial” and “regulatory” certification, and differences between QMS Sector Specific requirements.

Using MedMMAP for MedAccred Certification

Learn how the Medical Manufacturers MedAccred® Accreditation Pathway (MedMMAP) program can assist businesses to evaluate and begin their MedAccred certification.

The Nuances of Additive Manufacturing for Highly Regulated Industries

This session willl address how SMEs can enter into the world of additive manufacturing.

Pivoting to MedDev with Boyd Corporation

Learn how Boyd Corporation could help your organization in its transition into the medical devices market.

Innovation, Miniaturization, and the Pathway to Get There - Powered by Accu-mold

Explore some of the ways to overcome manufacturing roadblocks when working with contract manufactures, specialty suppliers, or your own internal infrastructure.

How Additive Manufacturing Can Help Businesses make the Technical Pivot from Aerospace to Medical

Learn why AM may allow businesses to rapidly pivot from aerospace to medical, given similarities in material, processing, and stringent qualification processes.

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