Meetings

AAMI Meetings and Events

2015

February 4
Free Webinar

New FDA Tools for Medical Device Adverse Event Reporting

February 9–12
Orlando, FL

Quality System Requirements and Industry Practice

February 10
Webinar

Best Practices in Endoscope Reprocessing

March 4–6
Arlington, VA

Design Control Requirements and Industry Practice

March 11–13
Alexandria, VA

Human Factors for Medical Devices

March 23–25
Bethesda, MD

Integrating Risk Management into the Quality System

March 23–26
Boston, MA

Quality System Requirements and Industry Practice

March 26–27
Arlington, VA

Safety Assurance Cases for Medical Devices

April 1–2
Herdon, VA

AAMI/FDA S3 Challenge 2015

April 13–16
Sydney, Australia

Quality System Requirements and Industry Practice

April 15–17
Alexandria, VA

Process Validation Requirements and Industry Practice

April 22–24
Baltimore, MD

Regulatory Requirements for Software Validation in the Medical Device Industry (Regulatory Focus)

April 26
Baltimore, MD

Design Control: The Intersection of Human Factors, Industrial Design, and Risk Management

April 27–28
Arlington, VA

Corrective and Preventive Action Requirements and Industry Practice

April 27–30
Annapolis, MD

AAMI Sterilization Standards Week

April 29–30
Baltimore, MD

Advanced Human Factors

April 29–May 1
Arlington, VA

Purchasing Controls and Supply Chain Management

May 14–15
Arlington, VA

Risk Management and Human Factors

May 17–23

Healthcare Technology Management (HTM) Week

May 18–21
Alexandria, VA

Industrial Sterilization for Medical Devices

June 1–3
Copenhagen, Denmark

Process Validation Requirements and Industry Practice

June 1–4, 2015
Copenhagen, Denmark/ Malmö, Sweden

Quality System Requirements & Industry Practice

June 5–8
Denver, CO

2015 AAMI Annual Conference and Expo

June 15–17
Copenhagen, Denmark

Fundamental Statistical Tools and Methods for Quality Systems

June 15–17
New Orleans, LA

Design Control Requirements and Industry Practice

June 15–18
Bethesda, MD

Quality System Requirements and Industry Practice

August 26–28
Alexandria, VA

Human Factors for Medical Devices

August 31–September 3
Munich, Germany

Quality System Requirements and Industry Practice

September 14–17
San Diego, CA

Ethylene Oxide Sterilization for Medical Devices

September 16–18
Alexandria, VA

Integrating Risk Management into the Quality System

September 21–24
Arlington, VA

Quality System Requirements and Industry Practice

September 28–October 1
Arlington, VA

Radiation Sterilization for Medical Devices

October 6–7
Arlington, VA

Effective Application of Agile Practices in the Development of Medical Device Software

October 7–9
Orlando, FL

Process Validation Requirements and Industry Practice

October 14–16
Las Vegas, NV

Developing and Validating Software for the Medical Device Industry (Practical Focus)

October 19–22
Silver Spring, MD

AAMI Sterilization Standards Week

October 21–23
Alexandria, VA

Design Control Requirements and Industry Practice

October 26–29
Arlington, VA

Quality System Requirements and Industry Practice

November 4–6
Arlington, VA

Human Factors for Medical Devices

November 16–17
Copenhagen, Denmark

Corrective and Preventive Action (CAPA) Requirements and Industry Practice

November 18–20
Copenhagen, Denmark

Design Control Requirements and Industry Practice

December 2–4
San Francisco, CA

Design Control Requirements and Industry Practice

December 7–10
Arlington, VA

Quality System Requirements and Industry Practice

2016

June 3–6
Tampa, FL

2016 AAMI Annual Conference and Expo

2017

June 9–12
Austin, TX

2017 AAMI Annual Conference and Expo