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Event Name Location Attendance Dates
2016 PDA Visual Inspection Interest Group Workshop 2016 PDA Visual Inspection Interest Group Workshop Bethesda, MD 125

05/18/2016 - 05/18/2016

PLM Road Map 2016 for the High Tech & Medical Device Industries PLM Road Map 2016 for the High Tech & Medical Device Industries Santa Clara, CA 300

05/24/2016 - 05/24/2016

Canada Talks Pharma 2016 Canada Talks Pharma 2016 Montreal, QC 300

05/25/2016 - 05/26/2016

AAMI 2016 Conference & Expo - Association for the Advancement of Medical Instrumentation AAMI 2016 Conference & Expo - Association for the Advancement of Medical Instrumentation Tampa, FL 2,200

06/03/2016 - 06/06/2016

Pre-Filled Syringes West Coast Pre-Filled Syringes West Coast San Diego, CA 100

06/06/2016 - 06/07/2016

Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing San Francisco, CA 30

06/06/2016 - 06/07/2016

Reduce R&D Costs by Simplifying Procurement: Enhance Efficiency, Increase Compliance and Save Costs Reduce R&D Costs by Simplifying Procurement: Enhance Efficiency, Increase Compliance and Save Costs Online Event n/a

06/08/2016 - 06/08/2016

2016 BIO International Convention - Biotechnology Industry Organization 2016 BIO International Convention - Biotechnology Industry Organization San Francisco, CA 15,700

06/06/2016 - 06/09/2016

Waste360 Healthcare Waste Conference 2016 Waste360 Healthcare Waste Conference 2016 Las Vegas, NV 13,000

06/08/2016 - 06/09/2016

Pharmapack North America 2016 Pharmapack North America 2016 New York, NY n/a

06/14/2016 - 06/15/2016

7th Digital Pharma West 7th Digital Pharma West Burlingame, CA 250

06/13/2016 - 06/15/2016

What is required to do for American manufacturers in order to comply with Canadian regulations? What is required to do for American manufacturers in order to comply with Canadian regulations? Online Event n/a

06/15/2016 - 06/15/2016

ISO 13485 2016 Quality management systems - Requirements for regulatory purposes  - By AtoZ Compliance ISO 13485 2016 Quality management systems - Requirements for regulatory purposes - By AtoZ Compliance Online Event n/a

06/15/2016 - 06/15/2016

MD&M East 2016 - Medical Device Manufacturing MD&M East 2016 - Medical Device Manufacturing New York, NY 10,500

06/14/2016 - 06/16/2016

OMTEC 2016 OMTEC 2016 Rosemont, IL 900

06/15/2016 - 06/16/2016

7th Aggregate Spend And Sunshine Act Summit 7th Aggregate Spend And Sunshine Act Summit Philadelphia, PA 600

06/15/2016 - 06/16/2016

Post-Market Compliance for Medical Devices and Evolving Reporting Requirements: Complaint Handling, MDR/eMDR and Recalls including UDI update Post-Market Compliance for Medical Devices and Evolving Reporting Requirements: Complaint Handling, MDR/eMDR and Recalls including UDI update San Diego, CA 30

06/16/2016 - 06/17/2016

Webinar on FDA Regulation of Medical Device Software Webinar on FDA Regulation of Medical Device Software Online Event n/a

06/23/2016 - 06/23/2016

From Market Compliance to Business Supply: The Necessity For Serialization From Market Compliance to Business Supply: The Necessity For Serialization Online Event n/a

06/28/2016 - 06/28/2016

Hemocompatibility:  Preclinical Biological Evaluation of Medical Devices for Interaction with Blood Hemocompatibility: Preclinical Biological Evaluation of Medical Devices for Interaction with Blood Online Event n/a

06/29/2016 - 06/29/2016

52nd DIA Annual Meeting - Drug Information Association 52nd DIA Annual Meeting - Drug Information Association Philadelphia, PA 7,500

06/26/2016 - 06/30/2016

Production and Process Controls for Medical Devices - By Compliance Global Inc. Production and Process Controls for Medical Devices - By Compliance Global Inc. Online Event n/a

06/30/2016 - 06/30/2016

Webinar on Update on Unique Device Identifier for Device Manufacturers Webinar on Update on Unique Device Identifier for Device Manufacturers Online Event n/a

06/30/2016 - 06/30/2016

Human Factors and Usability Studies - By Compliance Global Inc. Human Factors and Usability Studies - By Compliance Global Inc. Online Event n/a

07/06/2016 - 07/06/2016

A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences Online Event n/a

07/07/2016 - 07/07/2016

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