Come together. Work together. Do something meaningful.

What’s a Micro-Workshop?

Micro-workshops are free, virtual, interactive experiences, customized for your company. Different from webinars, these micro-workshops are hands-on and led by our best facilitators and topic experts. They are designed for small groups of around 10 people and are about 60-90 minutes long.

At the end of each micro-workshop, you’ll receive a customized output or report, capturing what you learned for future use.

You’ll collaborate in small groups. You’ll learn something new. You’ll get something done. You’ll move the needle. Join us!

Medical device manufacturers were already working on improving product quality, increasing compliance, and adapting to new healthcare business models.

But today, your priorities have shifted. You need ways to reduce near-term risk and transform your team, your capabilities, and your company to deal with future impacts. At the same time, you still need to run your business and take immediate actions to adapt and survive.

But where should you start?

How can you work now to enable a digital enterprise with integrated data that delivers innovative processes, products, and solutions for the next new normal? What actions can you take now to build resiliency for the future?

Free, Interactive Micro-Workshops for You and Your Industry

These are the micro-workshops currently available. Click “Sign Me Up” to let us know you’re interested. We’ll reach out to you to schedule a convenient time for you and your team.

MW Med Device QMS
Digital Quality Management System Assessment

This workshop will help you assess your company’s digital QMS maturity and prioritize top use cases.

Digital Quality Management System Assessment

How mature are your quality management capabilities? Is your organization compliance or quality focused? In this session, we’ll assess your company’s digital QMS maturity, prioritize top use cases to drive business value-add.

Who It's For

Best for directors in:

  • Quality & compliance
  • IT
  • R&D
  • Technology OCM
  • PLM IT

What You'll Get

You’ll receive a customized report benchmarking the maturity of your digital QMS capabilities and recommendations for your business on how to progress to the future state.

Sign Up: Digital Quality Management System Assessment

MW Med Device IOMT
Connected Device Strategy Diagnostic

This workshop will help you assess your IoMT use cases and end goals to determine your ideal connected device strategy.

Connected Device Strategy Diagnostic

If you have or are considering a connected device strategy, you need expertise in more than just FDA regulations – you also need to understand requirements for data transport and security. In this workshop, we will assess your IoMT use cases and end goals to determine the best options for how to approach connected devices, platforms, data and security.

Who It's For

Best for directors in:

  • R&D
  • Product development
  • Regulatory
  • Marketing

What You'll Get

You’ll receive a customized report on mitigating your connected device strategy risks and recommended next steps.

Sign Up: Connected Device Strategy Diagnostic

MW Med Device ARVR
What’s Your Highest-Potential AR/VR Use Case?

You’ll learn about the extended reality landscape and create an idea dashboard for your devices.

What’s Your Highest-Potential AR/VR Use Case?

AR/VR technologies have the potential to transform your productivity. But with potential use cases from work instructions to remote service to training, where will you get the most value? You’ll learn about the extended reality landscape and create an idea dashboard for your devices.

Who It's For

Best for directors in:

  • R&D
  • Service
  • Tech pubs
  • Tech support

What You'll Get

You’ll receive a customized report to help determine which device and which use case are your best AR/VR starting points.

Sign Up: What’s Your Highest-Potential AR/VR Use Case?

MW Med Device Regulatory
Regulatory Information Management (RIM) Maturity Assessment

In this session, you’ll learn about the benefits, scope and evolution of RIM (including registrations, submissions and tracking), and do a brief live maturity assessment of your organization’s capabilities.

Regulatory Information Management (RIM) Maturity Assessment

Regulatory information management systems are not new, but they have evolved to better support the global compliance requirements for life sciences companies. In this session, you will learn about the benefits, scope and evolution of RIM capabilities (including registrations, submissions and tracking), and do a brief live maturity assessment of your organization’s capabilities. We'll identify your as-is state and prioritize top RIM use cases that can drive additional business value.

Who It's For

Best for these levels in the regulatory function:

  • VP
  • Director
  • Manager

What You'll Get

You'll receive a customized report benchmarking the maturity of your RIM capabilities and recommendations for your business on how to progress to the future state.

Sign Up: Regulatory Information Management (RIM) Maturity Assessment