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Webinar On Risk Management and Risk-Based Monitoring

 
  December 11, 2014  
     
 


Compliance Trainings, Online
2015-02-02


Description :

This course provides an understanding of risk management principles and makes the links between study level risk management and the implementation of risk based monitoring.

New regulations with regard to Risk Based Monitoring were released by FDA in August 2013 to build on those for Quality Risk Management (ICH Q9) released in 2005 by ICH and 2006 by FDA. In addition there is permanent pressure on resources for clinical trials and it is vital that those precious resources are utilized there they deliver greatest benefit.

The implementation of risk-based study specific monitoring strategies, plans will be a critical component for every study sponsor to ensure high quality and integrity of data, enhance human subject protection, reduce cost and eliminate inefficiencies across clinical trial process. Thorough identification and evaluation of risks to critical study data, processes and thereby designing appropriate monitoring plan with a balance of centralized & onsite monitoring will maximize the effectiveness of risk based monitoring.

Considering the importance and need of risk-based monitoring currently in clinical trial management, it is recommended to attend this webinar that provides more insight on this new approach.

Areas Covered in the Session :

Regulatory requirement

Broad review of risk based activities

Study level risk management

RBM – adding value to your operations

What may generate risk?

Risk management documentation/risk statement structure

How to get started

Actions and how to manage them

Practical implications

Who Will Benefit:

A must attend webinar for all

Clinical Research Associates

Monitors

Data Management Team

Project Management Statisticians

Clinical Research Outsourcing

Drug Suppliers

All clinical research professional embarking on a risk-based approach

Price Tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email : support@compliancetrainings.com

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1254

 
 
Organized by: Compliance Trainings
Invited Speakers:

Speaker Profile

Over the past 28 years Jane has moved from routine data cleaning activities, via computer system validation onto training and data quality activities, eventually specializing in Quality Risk Management. Jane has worked for a variety of large pharmaceutical companies and CROs before retiring from GlaxoSmithKline. Jane now operates as a Risk Management Trainer and Consultant, specializing in Study Level Risk Management and Risk Based Monitoring as well as facilitation of risk assessment workshops.

 
Deadline for Abstracts: 2015-02-02
 
Registration:

 

https://compliancetrainings.com/siteengine/Login.aspx

E-mail: suzzane.d@compliancetrainings.com; uttam@compliancetrainings.com
 
   
 
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