home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
  HUM-MOLGEN -> Events -> Courses and Workshops  

Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner - Webinar by GlobalCompliancePanel

  September 22, 2010  

GlobalCompliancePanel, Online Training Webinar

Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.

Areas Covered in the Session:

  • Regulatory Requirements
  • Key Elements of a Supplier Qualification Program
  • Utilizing Quality Agreements
  • Supplier Assessment
  • Supplier Nonconformance
  • Required Documentation

Who Will Benefit: This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. The employees who will benefit include:

  • Purchasing management
  • Regulatory management
  • QA management
  • Consultants
Organized by: GlobalCompliancePanel
Invited Speakers: Jeff Kasoff, RAC, is the Director of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields. Jeff is responsible for oversight of corporate compliance with domestic and international regulations, preparation of submissions, and is primary liaison with regulatory agencies and notified bodies. Jeff has presented dozens of webinars in many areas dealing with regulatory compliance. Jeff began his regulatory career as the first full-time employee of Optex Biomedical, a device start-up, where he initiated their regulatory policies and procedures and prepared their submissions. Jeff received his Regulatory Affairs Certification in 1996.
Deadline for Abstracts: 2010-10-18

  Live live online training only for one participant
Price: $245.00

Corporate Live 4 to 10 participants from a single location (For multiple locations contact Customer Care) Price: $995.00

E-mail: webinars@GlobalCompliancePanel.com
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.