Medical Devices Webinars

• Jan 01, Thursday | 01:00 PM EST | 60 Mins

Risk management overarches projects associated with a particular product family, given that risks will both remain and c...

By JOSE IGNACIO MORA

• Jan 01, Thursday | 01:00 PM EST | 60 Mins

IEC 62304 is both a recognized consensus standard by the FDA and a harmonized standard in the EU; therefore, being compl...

By Don Hurd

• Jan 01, Thursday | 01:00 PM EST | 60 Mins

This event will help you to learn what the value of standards are including how and when to engage in the development an...

By

• Jan 06, Monday | 01:00 PM EST | 60 Mins

If you are constantly struggling to create, manage, and maintain all of the information found in the various Risk Manage...

By JOSE IGNACIO MORA

• Jan 06, Tuesday | 01:00 PM EST | 60 Mins

This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for compliant human factors/usab...

By JOSE IGNACIO MORA

• Jan 01, Thursday | 01:00 PM EST | 100 Mins

Internal audits are not just an important requirement for effective corporate governance – they are intended to sh...

By Frank Pokrop

• Jan 06, Tuesday | 01:00 PM EST | 60 Mins

Test method validation is an often-confusing requirement for medical devices. A fundamental issue is the role-reversal b...

By JOSE IGNACIO MORA

• Jan 01, Thursday | 01:00 PM EST | 60 Mins

FDA and the EU have tried to harmonize device regulatory requirements for over 25 years. Major differences between the F...

By CASPER ULDRIKS

• Jan 01, Thursday | 01:00 PM EST | 90 Mins

Internal Audit should be a key part of self-awareness and understanding strengths and weaknesses within your Quality Man...

By