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All Discussions Tagged 'medical' (72)

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Overview of Device Regulation – FDA 2017 Course "Overview of Device Regulation - FDA" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC re… Started by GlobalCompliance Panel	0	Apr 25
Risk Management in Medical Devices Industry 2017 Overview: Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products imposs… Started by GlobalCompliance Panel	0	Apr 25
Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements 2017 Course "Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements" has been pre-approved by RAPS … Started by GlobalCompliance Panel	0	Apr 25
Laboratory, Medical and Device Performance 2017 Course "Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines" has been pre-approv… Started by GlobalCompliance Panel	0	Apr 25
2017 FDA Data Integrity for Computerized Systems Seminar by GlobalCompliancePanel Overview: The Problem: We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Ann… Started by GlobalCompliance Panel	0	Feb 16
2017 FDA Data Integrity for Computerized Systems Seminar by GlobalCompliancePanel Overview: The Problem: We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Ann… Started by GlobalCompliance Panel	0	Feb 16
Supplier Management Conference for Medical Device Manufacturing in HONG KONG Overview: Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials a… Started by GlobalCompliance Panel	0	Jan 27
World Health Day - Prevent. Treat. Beat Diabetes This famous dictum is so true to today's stressful life. We are experiencing alarming rise of diseases like hypertension, diabetes, heart a… Started by HarNeedi	2	Nov 2, 2016 Reply by wlpwlp
FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices – GlobalCompliancePanel 2016 Overview: This seminar will show you how to structure and optimize your QMS. It all starts with Management Responsibility and a commitment… Started by GlobalCompliance Panel	0	Oct 20, 2016
Statistical Process Control & Process Capability – GlobalCompliancePanel 2016 Overview: This course teaches participants the fundamental concepts and methods needed to establish effective control charts and estimate p… Started by GlobalCompliance Panel	0	Oct 20, 2016