Earlier this year, I spoke with medical product liability expert and lawyer, Sara Dyson, on ways to reduce drug and device product liability risks through effective supplier due diligence and qualification … Continue reading at ComplianceZen.com →
From the Blog
Should FDA Regulate Medical Apps?
3D Printing and Nanobots – FDA Challenges
From the Pharma Contracting & Outsourcing Conference
Medical Apps and FDA Regulation
From the IMDA Medtech Conference
Client Success Stories
“John Avellanet was extremely helpful in assisting us to develop records and information management policies and records retention schedules that matched our FDA requirements and our resource capabilities. In addition, he managed our project expectations well and kept us on track and on budget.”
- Chih-Wu Chang, Senior Quality Manager, San Diego, California
