DEVELOPING AN EFFECTIVE 510 (K) APPLICATION STRATEGY IN A RESOURCE CONSTRAINED ENVIRONMENT

DEVELOPING AN EFFECTIVE 510 (K) APPLICATION STRATEGY IN A RESOURCE CONSTRAINED ENVIRONMENT ; PRODUCT INFO Includes 1 Hour Windows Media Video File and PowerPoint presentations for immediate download. PURCHASE VIDEO Innovative medical product companies are under...

HOW TO DECIDE WHEN A MODIFIED DEVICE REQUIRES A 510(K) CLEARANCE

HOW TO DECIDE WHEN A MODIFIED DEVICE REQUIRES A 510(K) CLEARANCE ; PRODUCT INFO Includes 1 Hour Windows Media Video File and PowerPoint presentations for immediate download. PURCHASE VIDEO Determining when a modification to a legally marketed device triggers the need...

HOW TO DECIDE WHEN A MODIFIED DEVICE REQUIRES A 510(K) CLEARANCE UNDER NEW FDA DRAFT GUIDANCES

HOW TO DECIDE WHEN A MODIFIED DEVICE REQUIRES A 510(K) CLEARANCE UNDER NEW FDA DRAFT GUIDANCES ; PRODUCT INFO Includes 1 Hour Windows Media Video File and PowerPoint presentations for immediate download. PURCHASE VIDEO Determining when a modification to a legally...

6th Annual Medical Device Regulatory Affairs: Securing Clearance & Maintaining Compliance Conference: Speaker Interview – Paul Swift/Alcon

Paul Swift Director, Global Regulatory Affairs Alcon   Paul will be one of the distinguished presenters at the 6th Annual Medical Device Regulatory Affairs: Securing Clearance & Maintaining Compliance Conference.   Why is the 6th Annual Medical Device...

6th Annual Medical Device Regulatory Affairs: Securing Clearance & Maintaining Compliance Conference: Speaker Interview – Larissa D’Andrea/ResMed

Larissa D’Andrea Director, Government and Regulatory Affairs ResMed   Larissa will be one of the distinguished presenters at the 6th Annual Medical Device Regulatory Affairs: Securing Clearance & Maintaining Compliance Conference.   Why is the 6th Annual...