Connect with a Regulatory Affairs Specialist
Practical RA provides regulatory affairs support for medical devices and in vitro diagnostic medical devices (IVDs), including Australian Sponsor services, EU MDR / IVDR consulting, US FDA support, and regulatory strategy.
Use this page to contact us to discuss your regulatory requirements or to arrange an initial discussion.
Contact Practical RA
Our team of experts will review your enquiry and respond within two business days.
Or, book an introductory call
For manufacturers who prefer to speak directly, you may also book a free introductory call with a regulatory specialist.
Our goal is to understand your regulatory requirements and determine whether Practical RA is able to support you.
There is no obligation to proceed following this discussion.
What Happens Next
- We review your enquiry to understand your device and regulatory needs
- A regulatory specialist will respond to clarify scope or request additional information
- Where appropriate, we will suggest an initial call to discuss next steps
Practical RA works with device manufacturers all over the globe provding structured, practical regulatory support. We focus on clarity, regulatory compliance, and realistic execution aligned with current regulatory expectations.