Effective Supplier Qualification Program - 2017

MessageThis Webinar is over
Date Aug 3, 2017
Time 10:00 AM
Cost 150.00
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"

Supplier Agreements, Quality Agreements and other documentation

including Audits/Assessments

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

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


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