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Clinical Compliance Conferences

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>Conference documentation and webinars for this Sector

How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial

Understanding of IRB application components and how to find out and fix problem areas before it threaten your trial to fail.

By : Compliance Online
Product Type : On Demand Webinar
Analytical Test Methods Validation: FDA, ICH and USP Requirements - Webinar

This training will address the regulatory requirements which apply at the various stages of development, and suggest proven strategies for compliant and phase-appropriate analytical method validation.

By : Compliance Online
Product Type : On Demand Webinar
Trial Master File for Research Sites: Can You Pass FDA Inspection?

This course reviews the investigator TMF required and additional content for a clinical trial - the activities of set-up, maintenance, and quality control and assurance will be discussed, as well as common deficiencies and challenges.

By : Compliance Online
Product Type : On Demand Webinar
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial

This clinical trial audit webinar will help with preparing the site and the study team with how to successfully prepare for an audit, how to identify risk of noncompliance, what to do before, during and after an audit.

By : Compliance Online
Product Type : On Demand Webinar
Clinical Statistics for Non-Statisticians. An Introduction to Statistical Concepts and Practices-Webinar

In this Clinical Statistics webinar/training all topics will be taught from a practical, non-theoretical perspective for non-statisticians & value and meaning of descriptive statistics including the use of normal vs. non-normal statistics.

By : Compliance Online
Product Type : On Demand Webinar

> Previous Conferences, Webinars and Training All Past Conferences >

Predictive Analytics World San Francisco 2016

Predictive Analytics World for Business is the leading event for predictive analytics professionals and managers. Register by Dec 18, 2015 and save $600. Take $150 off Early Bird or Two Day Pass fee by using discount code: CFS150 when registering.

By : Predictive Analytics World

3 Apr, 2016 - 6 Apr, 2016
California / San Francisco
FDA Inspection Lessons Learned: Lack of Trial Oversight

Critically assess the number of major and critical 2012 inspection findings related to trial oversight. Identifying regulatory requirements for appropriate delegation of duties and investigator oversight.

By : Compliance online

13 Jan, 2016 - 13 Jan, 2016
California / Palo Alto
From Biomarker to In-Vitro (Companion) Diagnostic Device: How to Design and Conduct Efficient Analytical Validation Studies in Accordance with CLSI Guidelines

This free webinar will introduce biomarker, in-vitro diagnostic devices and analytical validation terminology. The analytical validation in practice for the most important performance characteristics and how these should be established according to the recent CLSI guidance docs will be discussed

By : Xtalks Life Science Webinars

19 Oct, 2015 - 19 Oct, 2015
Canada / Toronto