One award available.
If you’re an entrepreneur in MedTech, Pharmaceuticals, IVD or software as a medical device (SaMD/SiMD), you’ll want to set the stage for compliance early on.
This opportunity to participate in our program is aimed at early-stage, pre-commercial startups that need Quality and Regulatory Support and/or Procedures covering key aspects of early activity in a concise fashion. There are key FDA Quality System Regulations and EU/MDR ISO 13485 medical device requirements to address processes and procedures for product development. In our experience of helping early stage innovators, we have found these business processes required to support compliance also create a foundation that investors depend on for de-risking their investment. To support these needs, this program will help you get a QMS set up for your pre-commercial enterprise with the support of CQG’s experts.
What does the program offer:
- Monthly – 60-minute Individual Expert Meetings with a Quality/ Regulatory Assurance Expert
- First 9 Procedure Templates Provided (Design & Development, Doc control, Material Controls, Nonconforming materials, Purchasing, Risk Management, Software Development, Supplier Quality, Training)
- Proprietary QS Dashboard Template Provided
Wherever you are in your venture, our goal is to help you get your innovative solutions to patients. We will support and guide you in the compliance requirements while you make it through the current environment of longer timeframes for funding and clearance. This program will help you make progress in the meantime in order to help you get your products to patients safely and efficiently and stick to your timelines. You can learn more by contacting us today at quality@cannonqg.com.
