Effective Supplier Qualification Program - 2017

  • Check with publisher
  • Published date: June 14, 2017
    • Fremont, California, United States

Overview:
FDA considers the supplier as an extension of your operation. You are liable
for supplier’s conduct. FDA will deal with your company in case of product
failure, especially as related to end user or patient safety concerns.

Areas Covered in the Session:
Learn the pre-selection, selection and assessment process through the use
of various tools
Methods, techniques and strategies that work and are proven with supplier
relations and qualification
Learn how to apply risk-based approaches and why and how to "rank" suppliers
Supplier Agreements, Quality Agreements and other documentation including Audits/Assessments

Who Will Benefit:
QA/QC/Compliance/Regulatory Affairs
Engineering/R&D/Technical Services
Purchasing/Procurement/Sourcing
Consultants

Speaker Profile:
David R. Dills,Global Regulatory Affairs & Compliance Consultant currently provides regulatory affairs and compliance consultative services for early-stage and established Class I/II/III device, IVD, biopharmaceutical, cosmetics and nutraceutical manufacturers on the global landscape, and has an accomplished record with more than 27 years of experience in the areas of Regulatory Affairs, Compliance and Quality Systems.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501324LIVE?channel=marketplace_Aug_2017_SEO

Compliance4All
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