All 2017 Events (17)

April 13Thursday

Introduction to Industrial Statistics 2017

April 13, 2017 at 9am to April 14, 2017 at 6pm – Salt Lake City, UT Overview: This is an introductory course in industrial statistics that will equip the attendee to understand what he or she needs to know about basic descriptive statistics such as measurements of c… Organized by NetZealous DBA as GlobalCompliancePanel | Type: introduction, to, industrial, statistics, 2017
New FDA FSMA Rules and Food Safety Controls 2017

April 13, 2017 at 9am to April 14, 2017 at 6pm – Baltimore, MD Course "Preparing to Comply with the New FDA FSMA Rules: Planning Valid Preventive Food Safety Controls" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC re… Organized by NetZealous DBA as GlobalCompliancePanel | Type: new, fda, fsma, rules, and, food, safety, controls, 2017
Quality by Design - Essential Techniques for Medical Devices 2017

April 13, 2017 at 9am to April 14, 2017 at 6pm – Salt Lake City, UT Overview: Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet, Design Controls are still one of the… Organized by NetZealous DBA as GlobalCompliancePanel | Type: quality, by, design, -, essential, techniques, for, medical, devices, 2017

April 20Thursday

Overview of Device Regulation – FDA 2017

April 20, 2017 at 8:30am to April 21, 2017 at 5:30pm – San Diego, CA Overview: This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers gui… Organized by NetZealous DBA as GlobalCompliancePanel | Type: overview, of, device, regulation, –, fda, 2017
Applied Statistics for FDA Process Validation 2017

April 20, 2017 at 9am to April 21, 2017 at 6pm – San Diego, CA Course "Applied Statistics for FDA Process Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: In… Organized by NetZealous DBA as GlobalCompliancePanel | Type: applied, statistics, for, fda, process, validation, 2017

April 27Thursday

Implementing ISO 13485:2016- 2017 by Dan O'Leary

April 27, 2017 from 8am to 6pm – Raleigh, NC Overview: The final version of ISO 13485:2016 is now available and companies should be planning their implementation. There are significant changes from the earlier version; they will require major… Organized by NetZealous DBA as GlobalCompliancePanel | Type: implementing, iso, 13485:2016-, 2017, by, dan, o'leary
Leadership Management Academy 201-202- 2017

April 27, 2017 at 8:30am to April 28, 2017 at 5:30pm – Raleigh, NC Overview: Why Should You Attend? By attending, you will take advantage of a great opportunity to advance as a manager to the next level! Too often, we focus on getting things done and results and mi… Organized by NetZealous DBA as GlobalCompliancePanel | Type: leadership, management, academy, 201-202-, 2017
Medical Devices Industry and Risk Management 2017

April 27, 2017 at 9am to April 28, 2017 at 6pm – Seattle, WA Overview: Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed sinc… Organized by NetZealous DBA as GlobalCompliancePanel | Type: medical, devices, industry, and, risk, management, 2017
Conducting Internal Investigations 2017

April 27, 2017 at 9am to April 28, 2017 at 6pm – Raleigh, NC Why should you attend : It seems that employees love to complain about anything, and it seems impossible to investigate everything. When employees feel, however, that you are not taking their compla… Organized by NetZealous DBA as GlobalCompliancePanel | Type: conducting, internal, investigations, 2017
Preparing Premarket Submissions that secures U.S. FDA Clearances/Approvals 2017

April 27, 2017 at 9am to April 28, 2017 at 6pm – San Diego, CA Overview: This workshop style training course is designed based on 30 year of regulatory affairs experience in preparing more than 150 successful U.S. FDA submissions for major medical device compan… Organized by NetZealous DBA as GlobalCompliancePanel | Type: preparing, premarket, submissions, that, secures, u.s., fda, clearances/approvals, 2017