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    Business Process Optimization in Pharmacovigilance - Webinar By GlobalCompliancePanel

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    Website http://www.globalcompliancepanel.com | Want to Edit it Edit Freely

    Category online training,Pharmacovigilance,Project structure,Business Process Management,compliance, safety perspectives,Business Process Optimization

    Deadline: March 15, 2012 | Date: March 15, 2012

    Venue/Country: online training webinar, U.S.A

    Updated: 2012-02-24 16:39:33 (GMT+9)

    Call For Papers - CFP

    Overview: This webinar will describe how to assess and optimize Pharmacovigilance operations from cost effective, compliance, and safety perspectives. A structured methodology for assessing drug safety operations will be presented. This will include recognizing the need to conduct process analysis, developing and prioritizing project portfolio, performing the analysis, and finally implementing the findings.

    The methodology has helped companies increase compliance at reduced cost. The scope covers all Pharmacovigilance activities: case processing activities such as case intake, data entry, assessment and reporting and signaling activities such as signal detection, evaluation and risk management.

    Areas Covered in the Session:

    Current Pharmacovigilance Environment

    Issues facing biopharmaceuticals

    Key pharmacovigilance Business Process Areas

    Detailed pharmacovigilance Issues

    Managing Business Processes

    Overview of Pharmacovigilance process

    High-level reference business process for Case processing and signaling

    Pharmacovigilance business process maturity

    Why Optimization follows Improvement

    Importance and role of metrics

    Framing the business process improvement - case for action

    Project structure ? who and when to involve

    Business Process Management ? what it is and why is it important

    How to Improve and Optimize Case Processing

    Planning - the first step

    Control - the final say

    Process Improvement Methodology - assessment and improvement

    Assessing case processing - flow charts and pain points

    Improving case processing - identify redundancies, duplications, multiple inspections, mismatched accountabilities and responsibilities

    Optimizing case processing - Allocating activities to resources

    Simulation and dynamic optimization - what-if scenarios

    Implementation challenges

    How to Optimize Signaling

    Reference Pharmacovigilance Process

    Impact of size of company

    Planning Signaling Operations

    Signal detection process optimization

    Signal evaluation process optimization

    Risk management process optimization

    Timing and frequency of signal detection, triage, and data mining runs

    Learning Objectives:

    Assess current Pharmacovigilance environment - case processing and signaling

    Identify areas of improvements - redundancies, automating manual intensive operations, over/under inspections

    Implement metrics and organization change management, including critical success factors

    Identify obstacles to implementation

    Evaluate pros and cons of outsourcing / off-shoring

    Who Will Benefit:

    Clinical Safety/Pharmacovigilance

    Quality Management

    Clinical Research & Development

    Price List:

    Live : $245.00

    Corporate live : $995.00

    Recorded : $295.00

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Phone: 800-447-9407

    Fax: 302-288-6884


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.