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    Best Practices for Quality Risk Management for Pharmaceutical Industry

    View: 211

    Website https://compliance2go.com/product/?pid=CP2014-391 | Want to Edit it Edit Freely

    Category Biotechnology , Food Safety Compliance , Medical Device , Pharmaceutical

    Deadline: November 12, 2014 | Date: November 12, 2014

    Venue/Country: Houston, U.S.A

    Updated: 2014-10-31 19:01:05 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    Firms in pharmaceuticals including those manufacturing biosimilars and biologics, who are intending to bring products into the US market, are subject to quality risk management (QRM).

    This presentation is intended to help you get familiar with best practices for the QRM applicable for pharmaceutical industry (drugs, biosimilars, and biologics).

    This seminar is further intended to discuss how quality risk management can be effectively integrated into a quality system (QS) in the pharmaceutical industry.

    This seminar will help attendees understand risk management principles, risk management tools, methods and processes applicable to the pharmaceutical industry. In addition, this seminar will help the attendees how to develop and implement a systematic and holistic risk management strategy integrated into the quality system.

    This 60-min webinar will provide great opportunities for you to get familiar with the details of how to implement the systematic and holistic quality risk management for drugs, biosimilars and biologics.

    Why should you attend :

    This webinar is intended to help you learn and ensure you can adequately implement quality risk management (QRM) applicable for pharmaceutical industry (drugs, biosimilars, and biologics).

    Areas Covered in the Session:

    Laws, Regulations, Rules and/or Standards

    Definitions

    Risk Management (RM) Process ? Systematic and Integrated

    RM Principles

    Risk Management Tools and Methods

    Risk Ranking

    How to Facilitate Quality Risk Management

    Common Mistakes and How to Prevent Common Pitfalls

    Risk Control Measures

    Risk Communication ? How

    RM Applications for Operations, R&D, Materials, Facilities, Utilities, Equipment, Manufacturing, Labeling and Packaging, Laboratory Studies and Quality Control.

    Doing RM Right Without Wasting Resources

    Practical Aspects (Value) of Risk Management

    Relationship with Other Quality Subsystems

    Common Pitfalls and Misconception

    How to Avoid Common Mistakes

    Implementing RM in an Efficient and Effective Manner.

    Speaker’s Practical PASS-IT Guide?

    Who will benefit: (Titles)

    CEOs

    VPs

    Compliance officers

    Attorneys

    Clinical affairs (associates, specialists, managers, directors or VPs)

    Regulatory affairs (associates, specialists, managers, directors or VPs)

    Quality assurance (associates, specialists, managers, directors or VPs)

    R&D (engineers, scientists, managers, directors or VPs)

    CROs

    Consultants

    Contractors/subcontractors

    Webinar Includes:

    Q/A Session with the Expert to ask your question

    PDF print only copy of PowerPoint slides

    60 Minutes Live Presentation

    Certificate of Attendance


    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.