how the process works
Make a request
Understanding regulatory, IVDR, and ISO 15189 compliance requirements can be complex. Our process is designed to identify gaps quickly and provide the right expertise to address them.
- Submit Your Requirements
Tell us about your challenge, project, or compliance needs.
- Expert Team Assignment
Our administration team assembles a multidisciplinary team of clinical, scientific, and regulatory experts best suited to your project.
- Proposal & Project Plan
We provide a detailed proposal outlining the scope of work, timelines, assigned personnel, deliverables, and projected costs.
- Project Delivery
Once approved, we commence the project and work collaboratively to deliver the agreed outcomes efficiently and compliantly.
Our goal is simple: identify the gaps, provide the expertise, and deliver practical solutions that help you achieve compliance and accelerate implementation.
Ordering & Payment
Products
A Purchase Order (PO) is required for all product orders. Invoices are issued upon delivery and are payable within 30 days.
Consultancy & Services
A proposal outlining scope, timelines, and costs will be provided before work begins. Services are delivered by our network of experienced clinical, scientific, and regulatory consultants.
Online Training
Payment is required at the time of registration to secure your place on the course.
Questions?
Contact us to discuss your requirements and receive a tailored proposal.
