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    Establishing a Reduced Testing Process for Incoming Materials

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    Website http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500481?expDate=Ourglocal | Want to Edit it Edit Freely

    Category Certificate of Analysis, cGMP regulations, FDA 21 CFR Regulations, GMP Standard, Material Qualification, Medical Device Components, Pharmaceutical Testing, Supplier History, Supplier Qualification, Trending

    Deadline: September 24, 2014 | Date: September 24, 2014

    Venue/Country: 38868 Salmon Ter, Fremont, U.S.A

    Updated: 2014-09-16 19:03:08 (GMT+9)

    Call For Papers - CFP

    Instructor: Howard T Cooper

    Description:

    The first step in reduced testing is to qualify the supplier using the supplier qualification process. This webinar will review the supplier qualification process.

    The sequential steps for establishing reduced testing program will be presented in a logical way using graphics including flowcharts. Guidance and recommendations for assessing the data to qualify a supplier for reduced testing will be discussed. This will be followed by describing the monitoring process to assure the required reliability. Considerable use of graphics will be used. Additionally, the basic quality principles that apply to reduce testing will be emphasized.

    Why Should you Attend:

    To increase understanding of requirements

    To learn how to maintain compliance and increase quality

    To gain insight for improving supplier quality while reducing cost and gaining resources that can be applied to quality, product, and process quality.

    Objectives of the Presentation:

    Introduction

    The role of materials in the achievement of product quality and customer satisfaction

    Similarities and differences of regulatory requirements for pharmaceutical, medical device, dietary supplements and food.

    Types of quality certificates

    A brief overview of supplier selection and qualification

    Material and laboratory qualification

    Material validation

    Collaborative testing between you and your supplier

    Factors to consider in establishing the sample plan to reduce risk

    The sampling plan calculation based primarily on risk factors

    Monitoring analytical results

    Taking corrective action

    Working with the supplier

    Supplier disqualification

    Going beyond reduced testing to supplier certification

    FDA compliance activities related to reduced testing

    Who can Benefit:

    QA, QC

    Laboratory

    Receiving warehouse

    Cost Accounting

    External Auditing

    Quick Contact:

    http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500481?expDate=Ourglocal

    Toll free: +1-510-857-5896

    Email:?webinaratonlinecompliancepanel.com

    OnlineCompliancePanel LLC,

    38868 Salmon Ter,

    Fremont, CA 94536, USA


    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.