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Best Practices for Lean Supplier Management in Compliance with FDA and ISO 13485 Requirements

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Category Supplier Evaluation and assessment, medical device quality requirements, medical device supplier evaluation, medical device supplier, quality system regulation, ISO 13485 requirements, medical device compliance, FDA medical device requirements, FDA medical device regulations, ISO 13485, device regulations, assessing medical device suppliers, assessing medical device vendors, supplier CAPA, supplier related corrective action

Deadline: December 05, 2017 | Date: December 06, 2017

Venue/Country: Online, U.S.A

Updated: 2017-11-14 21:44:19 (GMT+9)

Call For Papers - CFP

This webinar will review in detail the FDA QSR and ISO requirements for supplier evaluation and assessment, and discuss cost effective options for many of the common practices for achieving compliance.

Objectives of the Presentation:

Supplier Selection

Review of FDA and ISO requirements

Types of suppliers that must be qualified

Defining critical suppliers

Outsourced processes

Recommended Practices

Supplier Assessment

Review of FDA and ISO requirements

Recommended practices

Justification of desktop audits

Documentation requirements

For Registration:


Note: Use Promo Code HYED6Z and get 10% off on registration (Valid till DECEMBER 31st 2017)

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.