Webinar on “Risk-Based Monitoring: A Pathway to Efficient Quality Management” (Part II) : 5th June 2013; 11:00 – 12:00 hrs US EST

Part II: Risk-Based Monitoring – Putting into Practice

In order to maximize benefits of Risk Based Monitoring (RBM), the drug / device development companies, CROs are actively looking into implementation of it into practice. After getting proper perspectives on RBM, it is utmost important to have a right start to put RBM into practice to ensure effective use of RBM approach. Along with identification and evaluation of risks to critical study data & clinical trial operations,   it is very imperative to ponder over processes structuring, people alignment and necessary technology requirements to ensure high quality of data, enhance human subject protection, reduce cost and build high efficiencies across clinical trial processes.

After overwhelming response to Part I: Risk-Based Monitoring – Putting into Context, MakroCare takes pleasure to present the Part II  of this webinar.

Key Topics:
Part II : Risk-Based Monitoring – Putting into Practice

  • What may generate risk?
  • Risk management documentation/risk statement structure
  • How to get started
  • Actions and how to manage them
  • Practical Implications

Speakers:

Jane Tucker
Independent Risk Management Consultant and Trainer, UK

Jane_Tucker

Sue Fitzpatrick
Head of Education and Training
The Institute of Clinical Research, UK

Sue_Fitzpatrick

Facilitator

Ashok K. Ghone, PhD
VP, Global Services
MakroCare, USA

Ashok_Ghone

Date & Time :
Date : Wednesday, 5th June 2013
Time : 11:00 – 12:00 hrs US EST /16:00 – 17:00 hrs UK BST

Cost : None

Click Here to Register for Webinar or sent an e-mail to webinar@makrocare.com

For More Information Click Here

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