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Clinical Compliance Conferences

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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
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
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
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

> 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