Sign for Notice Everyday    Sign Up| Sign In| Link| English|

Our Sponsors

    Receive Latest News

    Feedburner
    Share Us


    Best Practices for Quality Risk Management for the Pharmaceutical Industry. - By Compliance Global Inc

    View: 221

    Website https://www.complianceglobal.us/product/700130 | Want to Edit it Edit Freely

    Category risk management plans, risk management plan, risk management in healthcare, risk management process, risk management tool, fda approval process, fda cfr, fda regulations, compliance fda, fda compliance program, risk management plan, risk assessment plan, operational risk management, risk analysis, risk assessment tool, lab tests, lab tests online, lab test online, laboratory testing, lab values, lab work, lab technician

    Deadline: June 30, 2015 | Date: June 30, 2015

    Venue/Country: New Hyde Park, U.S.A

    Updated: 2015-05-28 18:13:33 (GMT+9)

    Call For Papers - CFP

    Overview:

    This webinar is intended to help you better understand and get familiar with best practices for FDA approval process for quality risk management (QRM) applicable for pharmaceutical industry (drugs, biosimilars, and biologics). The contents of this webinar is also highly applicable to the medical device industry.

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

    This webinar will help attendees understand risk management principles, risk management tools, methods and processes applicable to the pharmaceutical industry. In addition, this webinar 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 webinar, the speaker will guide you through the details of how to implement the systematic and holistic risk management for drugs, biosimilars and biologics.

    The speaker will walk you through the best FDA compliant practices.

    Why Should You Attend:

    To get familiar with the FDA compliant risk management plans and practices.

    Areas Covered in the Session:

    Applicable Laws and Regulations

    ? Key Definitions

    ? Risk Management (RM) Process ? Systematic and Integrated

    ? RM Principles

    ? 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 Testing and Quality Control

    ? Doing RM Right Without Wasting Resources

    ? Practical Aspects (Value) of Risk Management

    ? Relationship with Other Quality Subsystems

    ? Implementing RM in an Efficient and Effective Manner

    ? Speaker’s Practical PASS-IT Guide

    Learning Objectives:

    To better understand and establish quality risk management practices.

    Who Will Benefit:

    ? Regulatory Affairs

    ? Quality Professionals

    ? R&D Professionals

    ? Complaint And Risk Management Personnel

    ? Consultants

    ? Contractors/Subcontractors

    ? CEO’s

    ? VP’s

    ? Compliance Officers

    ? Attorneys

    ? Clinical Affairs Personnel

    ? Other Interested Parties

    Level:

    Intermediate

    For more detail please click on this below link:

    https://www.complianceglobal.us/product/700130

    Email: referralsatcomplianceglobal.us

    Toll Free: +1-844-746-4244

    Tel: +1-516-900-5515


    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.