Article Ontogen Medtech 11/1/23 Article Ontogen Medtech 11/1/23 NIH / NSF SBIR Grant Success Rates Read More Article Ontogen Medtech 5/5/23 Article Ontogen Medtech 5/5/23 Demystifying FDA Medical Device Classification: A Comprehensive Guide Read More Article Ontogen Medtech 2/27/23 Article Ontogen Medtech 2/27/23 30 Medical Device Acronyms You Should Know Read More Article Ontogen Medtech 2/3/23 Article Ontogen Medtech 2/3/23 What is Document Control and why is it necessary? Read More Article Julie Byars 1/14/23 Article Julie Byars 1/14/23 Top 10 reasons for FDA 483 citations (Warning Letters) in medical devices in 2022 Read More Article Tyler Panian 11/21/22 Article Tyler Panian 11/21/22 Cybersecurity for Medical Devices: an Overview Read More Article Tyler Panian 10/15/22 Article Tyler Panian 10/15/22 What is a traceability matrix and how is it used in medical device development? Read More Article Ontogen Medtech 9/1/22 Article Ontogen Medtech 9/1/22 Differences and Similarities Between De Novo Submission and 510(k) Pathway for FDA Medical Device Approval Read More Article Tyler Panian 10/3/21 Article Tyler Panian 10/3/21 Methods of Sterilizing Medical Devices: an Overview Read More Older Posts
Article Ontogen Medtech 11/1/23 Article Ontogen Medtech 11/1/23 NIH / NSF SBIR Grant Success Rates Read More
Article Ontogen Medtech 5/5/23 Article Ontogen Medtech 5/5/23 Demystifying FDA Medical Device Classification: A Comprehensive Guide Read More
Article Ontogen Medtech 2/27/23 Article Ontogen Medtech 2/27/23 30 Medical Device Acronyms You Should Know Read More
Article Ontogen Medtech 2/3/23 Article Ontogen Medtech 2/3/23 What is Document Control and why is it necessary? Read More
Article Julie Byars 1/14/23 Article Julie Byars 1/14/23 Top 10 reasons for FDA 483 citations (Warning Letters) in medical devices in 2022 Read More
Article Tyler Panian 11/21/22 Article Tyler Panian 11/21/22 Cybersecurity for Medical Devices: an Overview Read More
Article Tyler Panian 10/15/22 Article Tyler Panian 10/15/22 What is a traceability matrix and how is it used in medical device development? Read More
Article Ontogen Medtech 9/1/22 Article Ontogen Medtech 9/1/22 Differences and Similarities Between De Novo Submission and 510(k) Pathway for FDA Medical Device Approval Read More
Article Tyler Panian 10/3/21 Article Tyler Panian 10/3/21 Methods of Sterilizing Medical Devices: an Overview Read More
