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    THIS SEMINAR IS FURTHER INTENDED TO DISCUSS HOW QU 2015 - Webinar On Quality Risk Management for Drugs and Biologics

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    Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1515 | Want to Edit it Edit Freely

    Category Food, Drugs & Biologics

    Deadline: May 29, 2015 | Date: May 29, 2015

    Venue/Country: Mississauga, Canada

    Updated: 2015-05-11 15:40:09 (GMT+9)

    Call For Papers - CFP

    Description :

    This presentation is intended to help you get familiar with best practices for quality risk management (QRM) applicable to pharmaceutical industry (drugs, biosimilars, and biologics) as well as medical device industry.

    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.

    In this 60-min presentation, the speaker will guide you through the details of how to implement the systematic and holistic risk management for drugs, biosimilars, biologics and medical devices.

    Areas Covered in the Session :

    Laws and Regulations

    Key Definitions

    Risk Management (RM) Principles

    Risk Management Process ? Systematic and Integrated

    Risk Management Tools and Methods (PHA, HAZOP, HACCP, FTA, FMEA, FMECA)

    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

    Interfacing and Relationship with Other Quality Subsystems

    Best Practices for Implementing Quality Risk Management in an Efficient and Effective Manner.

    Speaker’s Practical PASS-IT Recommendations

    Who Will Benefit:

    CEOs

    VPs

    Compliance Officers

    Attorneys

    Complainant Managers

    Managers (RA, QA/QC, CA)

    Consultants

    Contractors and Subcontractors

    Anyone interested in the topic

    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 : supportatcompliancetrainings.com

    For more information about this event please visit

    https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1515


    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.