What’s the Role of Product Requirements in Sustainable Development?
Sharing monthly #product and #quality insights to help bring products to life.

What’s the Role of Product Requirements in Sustainable Development?

Requirements management is crucial to ensuring your product meets market needs and business goals and can play a key role in ensuring #sustainability. In this edition of the Arena Talk Newsletter, we go over the role of requirements management in #sustainable #productdevelopment, as well as:

  • tips on managing engineering and #manufacturing change orders
  • how to classify under the new EU #MDR and #IVDR
  • how to avoid BOM mistakes

... and more.

The Role of Product Requirements in Sustainable Development

Team discussing requirements management
Learn the role requirements management plays in sustainable product development.
"Effective requirements management makes sure new or improved products meet market needs and business goals. In other words, it’s key to a successful product company." - Ann McGuire

Emerging right-to-repair laws aim to increase product longevity by requiring manufacturers to provide consumers with the necessary documentation, tools, and service parts to make their own repairs.

Ann McGuire , Director of Product Marketing at Arena, a PTC Business, and Michelle Stone share their insights on using requirements management to develop sustainable products and what lies ahead with the new global push for right to repair.

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The Essential Guide to Engineering and Manufacturing Change Orders

Two engineers reviewing engineering change order
Cloud PLM and QMS can help streamline engineering and manufacturing change orders.

Ineffective change order management could spell disaster for your product launch.

Change orders specify modifications to a product’s design or manufacturing procedure. More importantly, they ensure that the final product meets required quality and performance standards and is produced efficiently and affordably.

Read this guide to learn the ins and outs of engineering and manufacturing change orders and how Cloud #PLM and #QMS streamlines the process.

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How to Classify Your Device Under the MDR and IVDR

Two women looking at medical device design
Medical device companies must know how to classify their products under the new EU MDR and IVDR.

A critical step in certifying your #medicaldevice under the European regulations is to ensure that it’s assigned the correct classification. This will help you identify product requirements early in the development phase and establish a roadmap for compliance throughout the entire lifecycle.

This article reviews the classification criteria established by the EU MDR and IVDR and provides steps on how to accurately classify your device.

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Avoiding BOM Mistakes

Arena Tip of the Month
Arena Tip of the Month: How to avoid BOM mistakes

Still managing your bill of materials (BOM) with spreadsheets?

An accurate BOM ensures cost-effective and compliant sourcing, maintains quality control, and speeds new product introduction.

Tip: Having an intelligent system that automatically links relevant documentation and change review processes to the product BOM can help you avoid costly mistakes.

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Solution Architect Scott Segrin Shares 3 Keys to a Successful QMS Implementation

Scott Segrin shares his insights for successful QMS implementation.
“I take the most pride in getting customers up and running to the point where they can advance their business.” - Scott Segrin

Today, medical device companies are realizing the benefits of investing in an enterprise #qualitymanagementsystem (eQMS) as they deal with more stringent regulations.

Arena Solution Architect Scott Segrin reveals how he helps customers adopt a Cloud QMS solution and shares tips for ensuring a fast and painless implementation.

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Quality & Regulatory Alignment for Audit Readiness

Laptop screen with webinar displayed
Learn how quality and regulatory alignment can help you prepare for audits.

Today, medical device companies are looking to better align their quality and regulatory teams and streamline the #audit experience.

In this webinar, Arena Customer Success Coach Christine Pompa and Rimsys Director of Regulatory, Bruce McKean , discuss how a shared data strategy between teams can enable successful interactions with regulatory authorities and limit audit findings.

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Expedite Cross-Functional Design Reviews

Global product teams and partners need a convenient way to optimize designs and speed development lead times.

See how the Arena 3D #CAD Viewer simplifies the review of 3D models to help you release cutting-edge products faster.

Arena Events and Tradeshows

Embrace a New Era of Product Development? ?

Learn the secrets of today’s thriving, collaborative product companies and the technologies they’re using to achieve agile, efficient, and connected product design and development.? ?

  • September 13, 2023?
  • 10 am PT, 1 pm ET?
  • Live Webinar

Register Now

DroneX Tradeshow & Conference

Join the UK’s largest drone event dedicated to UAV products and services. Take part in networking opportunities, keynotes, and live PLM demos from our industry experts.? ?

  • September 26-27, 2023?
  • Booth E94?
  • London, United Kingdom?

Join Us

RoboBusiness and DeviceTalks West?

Join this co-located event to learn how medical device and commercial robotics innovators are finding success in a challenging economic market. Visit our team in the Field Robotics Pavilion for a live demo of Arena PLM and QMS.?

  • October 18-19, 2023?
  • Booth 414?
  • Santa Clara, California

Join Us

EVE Tech Asia Exhibition & Conference?

See us at the premiere B2B show in Asia that features leading electric vehicle and environmental technology enterprises, infrastructures, battery manufacturers, IT solutions, and service providers.

  • November 22-24, 2023?
  • Booth D33?
  • Singapore

? Join Us

Want to keep up with the latest?PLM and QMS?news from Arena??Subscribe to our blog here.

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