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Event Name Location Attendance Dates
Responding to FDA - 483s (List of Observations) and Warning letters from FDA- By Compliance Global Inc. Responding to FDA - 483s (List of Observations) and Warning letters from FDA- By Compliance Global Inc. Online Event n/a

10/12/2016 - 10/12/2016

2nd World Congress And Exhibition On Antibiotics 2nd World Congress And Exhibition On Antibiotics Manchester 200

10/13/2016 - 10/15/2016

2016 AARC Congress - American Association For Respiratory Care 2016 AARC Congress - American Association For Respiratory Care San Antonio, TX 6,000

10/15/2016 - 10/18/2016

2016 PDA Drug Delivery Combination Products Workshop 2016 PDA Drug Delivery Combination Products Workshop Huntington Beach, CA 300

10/19/2016 - 10/19/2016

AAPM&R 2016 Annual Assembly & Technical Exhibition - American Academy of Physical Medicine & Rehabilitation AAPM&R 2016 Annual Assembly & Technical Exhibition - American Academy of Physical Medicine & Rehabilitation New Orleans, LA 2,400

10/20/2016 - 10/23/2016

Reprocessing Medical Devices: Approaches and Considerations for Manual Cleaning Validations Reprocessing Medical Devices: Approaches and Considerations for Manual Cleaning Validations Online Event n/a

10/26/2016 - 10/26/2016

FDA's Two New Draft Guidance on Software and Device Changes and the 510(k) - By AtoZ Compliance FDA's Two New Draft Guidance on Software and Device Changes and the 510(k) - By AtoZ Compliance Online Event n/a

10/26/2016 - 10/26/2016

New ISO 13485: Proposed Changes and What They Mean to the Medical Device Industry  - By Compliance Global Inc. New ISO 13485: Proposed Changes and What They Mean to the Medical Device Industry - By Compliance Global Inc. Online Event n/a

10/27/2016 - 10/27/2016

10th Annual Digital Pharma East 10th Annual Digital Pharma East Philadelphia, PA 800

10/24/2016 - 10/27/2016

Understanding Design Controls (To Include Adaptive Designs For Clinical Studies) - By AtoZ Compliance Understanding Design Controls (To Include Adaptive Designs For Clinical Studies) - By AtoZ Compliance Online Event n/a

11/01/2016 - 11/01/2016

How to prepare for and host a FDA inspection and respond to 483's - By Compliance Global Inc. How to prepare for and host a FDA inspection and respond to 483's - By Compliance Global Inc. Online Event n/a

11/01/2016 - 11/01/2016

Medtrade Fall 2016 Medtrade Fall 2016 Atlanta, GA 7,000

10/31/2016 - 11/03/2016

2016 PDA Outsourcing/CMO Conference 2016 PDA Outsourcing/CMO Conference Washington, DC 150

11/03/2016 - 11/04/2016

Pharma EXPO 2016 Pharma EXPO 2016 Chicago, IL 10,000

11/06/2016 - 11/09/2016

Supplier Management for Medical Device Manufacturers: 2-day In-person Seminar Supplier Management for Medical Device Manufacturers: 2-day In-person Seminar San Francisco, CA 30

11/10/2016 - 11/11/2016

Proposed Changes by FDA: Bullet Proof 510(k) Proposed Changes by FDA: Bullet Proof 510(k) Chicago, IL 50

11/10/2016 - 11/11/2016

FDA's Two New Draft Guidance on Software and Device Changes and the 510(k) FDA's Two New Draft Guidance on Software and Device Changes and the 510(k) Online Event n/a

11/15/2016 - 11/15/2016

Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs) Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs) San Diego, CA 30

11/17/2016 - 11/18/2016

Training by Compliance4all on How to Manage a Medical Device Recall Training by Compliance4all on How to Manage a Medical Device Recall Online Event n/a

11/21/2016 - 11/21/2016

Supply Chain Data Integrity - By AtoZ Compliance Supply Chain Data Integrity - By AtoZ Compliance Online Event n/a

11/23/2016 - 11/23/2016

Training by Compliance4all on Quality and Compliance for Medical Devices Training by Compliance4all on Quality and Compliance for Medical Devices Online Event n/a

11/29/2016 - 11/29/2016

Update on Global UDI Initiatives for Medical Devices - By Compliance Global Inc. Update on Global UDI Initiatives for Medical Devices - By Compliance Global Inc. Online Event n/a

11/29/2016 - 11/29/2016

U.S. FDA's Two New Draft Guidances on Device and Software Changes and the 510(k) - By Compliance Global Inc. U.S. FDA's Two New Draft Guidances on Device and Software Changes and the 510(k) - By Compliance Global Inc. Online Event n/a

11/30/2016 - 11/30/2016

Training by Compliance4all on Investigational Device Exemption Training by Compliance4all on Investigational Device Exemption Online Event n/a

12/01/2016 - 12/01/2016

FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices - GlobalCompliancePanel 2016 FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices - GlobalCompliancePanel 2016 Baltimore, MD 50

12/01/2016 - 12/02/2016

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