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Risk Management in Medical Devices Industry 2017Overview: 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 |
Quality by Design using Design of Experiments (QbD) 2017Course "Quality by Design using Design of Experiments (QbD)" has been pre-approved by RAPS as eligible for up to 12 credits towards a part… Started by GlobalCompliance Panel |
0 | Apr 25 |
HIPAA Compliance for Small Healthcare Providers 2017Overview: Being in compliance with HIPAA involves not only ensuring that you provide the appropriate patient rights and controls on your u… Started by GlobalCompliance Panel |
0 | Apr 25 |
World Health Day - Prevent. Treat. Beat DiabetesThis 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 |
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Nov 2, 2016 Reply by wlpwlp |
Master HIPAA Compliance in Six StepsOverview: The secret is - HIPAA Rules are easy and routine to follow - when they are explained step-by-step in plain language. In this semi… Started by GlobalCompliance Panel |
0 | Oct 20, 2016 |
Product Reliability Seminar 2016Overview: Although a primary objective of reliability analysis is to improve product reliability, there are many possible reasons for colle… Started by GlobalCompliance Panel |
0 | Sep 28, 2016 |
Clinical Research Seminar 2016: Current Regulations under FDA and HIPAAOverview: This two day seminar will provide the foundation for the application, concepts and theories of clinical research. Within the two… Started by GlobalCompliance Panel |
0 | Sep 28, 2016 |
Employee Selection Tools and Techniques 2016Overview: Employee selection and promotion is about predicting the future. At decision time, the questions to be answered are "How well wil… Started by GlobalCompliance Panel |
0 | Sep 28, 2016 |
Proposed Changes by FDA : Bullet Proof 510(k)Overview: This Two-day course is a primer and overview to the premarket notification process, i.e., a 510(k). A 510(k) is a premarket submi… Started by GlobalCompliance Panel |
0 | Sep 28, 2016 |
Statistical methods for Risk Management 2016Course "Applied Statistics, with Emphasis on Verification, Validation, and Risk Management, in R&D, Manufacturing, and QA/QC" has been… Started by GlobalCompliance Panel |
0 | Sep 28, 2016 |
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