Considerations for Building Your Own Cloud Device: Regulations, Privacy & Cybersecurity

Medical devices are becoming increasingly cloud-connected. What used to be a technology only deployed by the largest, most well-funded companies is now becoming a core requirement of most medical device startups. Developing cloud solutions can be a risky endeavor when considering privacy, security and regulation challenges.

Register for this free webinar presented by Abbas Dhilawala, CTO of Galen Data, who will describe these challenges and provide considerations that are critical for success. For companies developing devices with a cloud dependency, investors in medical device companies, or those who have a general interest in medical device innovation, please join us for this informative webinar and Q&A session.

Watch the webinar

Galen Data Webinar 7-28-22
Specifically, this webinar will cover:
  • What are the benefits of connected devices?
  • What are the hardware and software considerations of connecting a device to the cloud?
  • What are the regulatory, privacy, and cybersecurity considerations of connectivity?
  • How to decide between building or buying a connectivity solution.
Who should attend?
  • Medical Device Executives
  • Product Development and Engineering
  • Quality and Compliance Professionals
Register Now  

Hosted by

Abbas D 300x300
Presenter: Abbas Dhilawala

Chief Technology Officer,
Galen Data

Moderator: Etienne Nichols

Medical Device Guru & Community Manager, Greenlight Guru


galen data

About Galen Data

Galen Data, Inc. provides a turnkey cloud solution for medical device makers that is configurable, secure, and compliant. The company was founded to make device-to-cloud connectivity possible in a matter of weeks instead of months, and at a fraction of the cost as compared to custom developed solutions. The Galen CloudTM collects and securely stores data and includes tools to visualize and analyze that data. Dashboards and alerts for the manufacturer, medical team, and patients are also provided within the platform. The software platform is compliant to FDA, HIPAA, and CE Mark standards, and is ISO 13485:2016 certified. Visit their website to learn more.


About Greenlight Guru

Greenlight Guru is the only Medical Device Success Platform (MDSP) for companies to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based software, Greenlight Guru is easier to implement, easier to use and designed to fit all medical device needs to enable innovative, safe and effective, True Quality medical devices. Visit our homepage to learn more.

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