John Robinson #1549324

August 30, 2012

Device Corrections and Removals -Webinar By GlobalCompliancePanel at Online Training

October 4, 2012

Risk Management: ISO14971, IEC62304 and IEC60601-1: 2005 Compliance - Webinar By GlobalCompliancePanel at Courtyard San Diego Mission Valley/Hotel Circle

October 11, 2012

FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel at Online Training

October 16, 2012

Complaint Handling in Compliance with FDA and ISO Regulations - Webinar By GlobalCompliancePanel at Online Training

October 28, 2012

India Seminar 2012 at Mumbai - The A to Z's of Microbial Control, Monitoring, and Validation of Pharmaceutical Water Systems by Teri C. Soli at Intercontinental the Lalit

October 30, 2012

Update on Unique Device Identifier for Device Manufacturers - Webinar By GlobalCompliancePanel at Online Training

October 31, 2012

Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel at Online event

November 6, 2012

Pharmaceutical and Biologics Facility Design: FDA and Regulatory Aspects -Webinar By GlobalCompliancePanel at Online Training

November 6, 2012

21 CFR Part 11: Complying with Part 11 Regulation - Understanding the Predicate Rule - Webinar By GlobalCompliancePanel at Online Training

November 7, 2012

Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel at Online Training

November 8, 2012

The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations - Webinar By GlobalCompliancePanel at Online Training

November 8, 2012

Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) - Webinar By GlobalCompliancePanel at Online Training

November 13, 2012

Implementing Medical Device Complaint Handling Systems - Webinar By GlobalCompliancePanel at Online Training

November 13, 2012

Design Control for Professionals - Webinar By GlobalCompliancePanel at Online Training

November 13, 2012

Good Documentation Practices for GMP Operations - Webinar By GlobalCompliancePanel at Online Training

November 14, 2012

The DHF, DMR, DHR, and the Technical File-Design Dossier - USFDA and EU MDD Requirements - Webinar By GlobalCompliancePanel at Online Training

November 14, 2012

Combination Products: FDA's Proposed Rule for GMP Requirements and Introduction and Expectations for "Combo" Products - Webinar By GlobalCompliancePanel at Online Training

November 14, 2012

Statistical Procedures Needed for Compliance with the Guidance on Process Validation -Webinar By GlobalCompliancePanel at Online Training

November 14, 2012

Configuration Management and Change Control for Computer Systems - Webinar By GlobalCompliancePanel at Online Training

November 15, 2012

Lyophilization Process Development and Cycle Design with a Case Study - Webinar By GlobalCompliancePanel at Online Training

November 15, 2012

Process Validation Principles and Protocols for Medical Devices - Webinar By GlobalCompliancePanel at Online Training

November 15, 2012

Process Validation Principles and Protocols for Medical Devices - Webinar By GlobalCompliancePanel at Online Training

November 20, 2012

Obtaining an FDA Investigational Device Exemption - Webinar By GlobalCompliancePanel at Online Training

November 27, 2012

Current Good Manufacturing Practice for Medical Devices Including IVDs - Webinar By GlobalCompliancePanel at Online Training

November 27, 2012

Ensuring Integrity and Security of Electronic Records for FDA Compliance - Webinar By GlobalCompliancePanel at Online Training