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Clinical Compliance Conferences

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Fundamentals of FDA’s Clinical Trial Audits – A Must- Know for Audit preparation

This Clinical Trial Audits webinar will provide help both CRAs and sites utilize quality improvement methods and effectively prepare for upcoming GCP audits.

By : Compliance Online
Product Type : On Demand Webinar
How to secure GCP compliance in Clinical Trials

This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this, will translate GCP in a more practical, applied sense.

By : Compliance Online
Product Type : On Demand Webinar
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
3-hr Virtual Seminar - China: Compliance Processes for Life Science Products

This 3-hr virtual seminar on compliance processes for life science products in China will discuss the regulatory structure and requirements for compliance with Chinese SFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products.

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

> 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