Events In USA
Risk Analysis Techniques in Clinical Trials
This webinar will provide you with an overview of risk factors in clinical trials and discuss possible ways to mitigate, control, assess impact, and prevent them in your trial.
Statistics for the Non-Statistician
Statistics for the Non-Statistician - US Seminar 2012 at Washington DC
Best Technique for Clinical Trial Audit,Inspection
This webinar on clinical trial audit/ inspection preparedness will discuss in detail about applicable regulatory and sponsor requirements, guidelines and SOPs.
Big Design Conference 2012
Join experts in the fields of design, mobile, gaming, usability, strategy, content, multimedia, and film in Big D.
Device Corrections and Removals
This 90-minute webinar on device corrections and removals will clarify your obligations for corrections and removals under Part 806 of the FDA regulations.
Verification and Validation in the Medical Devices
This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices.
FDA Acceptance of non-US Clinical Trials
This webinar will help you understand how non-IND clinical trials at non-US locations can be used successfully to support an IND/IDE or a marketing approval application.
Medical Device - Mitigation through FMEA
This 90-minute presentation will discuss a structured way to mitigate risks with minimum cost. You will learn how to use FMEA to effectively estimate and assess risks in your medical device.
An Approach to Fair Lending and UDAAP
Current and future compliance professionals, lenders, loan originators, board of directors, senior management. Anyone responsible for the development, marketing, and sales of bank products .
Detection and Escalation in Clinical Trial Setting
This webinar on issue detection and escalation in clinical trial settings will review the responsibilities of sponsors, investigators, IRB in clinical trial setting to maintain compliance.
Acceptance Sampling by Variables Using Z1.9
This 90-minute webinar on sampling plans using ANSI/ASQ Z1.9 will explain the methods in Z1.9 and shows how to use it in a more modern setting (using simple statistical calculators).
Can You Pass FDA Inspection?
This webinar on Trial Master File (TMF) for clinical research sites will show how you can create an FDA compliant TMF to ensure that it will pass inspection by FDA investigators and QA Auditors.
UX Week 2012
UX Week is the premier user experience design conference. Design professionals from all over the world gather for four days of community, inspiration and skills building.
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