Date: | April 12, 2018 - 9:00am - April 13, 2018 - 4:00pm |
Timezone: | (GMT-05:00) Eastern Time (US & Canada) |
Location: | DoubleTree by Hilton Philadelphia Airport 4509 Island Avenue, Philadelphia, PA 19153, PA, PA, 19153, United States |
Website for Event: | https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901636S... |
Topic: | Health Education |
Description: | Course "Supplier Management in FDA- and ISO-regulated Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Why should you attend Notified bodies and the FDA cannot require your suppliers to meet the quality system regulations, so they must make sure you are exercising sufficient control over those suppliers. You must make sure your supplier management and system meets all required regulations and guidance documents, especially for outsourced processes such as contract manufacturing, sterilization and testing, and also for critical suppliers. Sure, you depend on your suppliers to provide you with goods and services, but can your system prove that you have sufficient control over your suppliers to assure auditors and regulatory agencies that your product is safe and meets all your requirements? Your supplier management program can be in compliance, but is it cost effective? If not, your unquantifiable overhead costs may be out of control. Is your supplier management program collaborative with your suppliers? If your company is too demanding of your suppliers, you risk alienating them or even worse losing them - try explaining that to your supply chain folks! Areas Covered in the Session: • Supplier Selection Who Will Benefit: This seminar will provide valuable assistance to all regulated companies that are interested in implementing and maintaining a supplier management program that is both compliant and cost-efficient. The employees who will benefit include: Agenda: Day 1 Schedule Lecture 1: Introduction Day 2 Schedule Lecture 1: Speaker Jeff Kasoff, RAC, CMQ/OE is the Principal Consultant at Lean to Quality, LLC. He s has more than 30 years of experience in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operations and assured compliance, at all sizes of company, from start-up to more than $100 million in revenue. This multi-faceted experience makes Jeff uniquely qualified to address compliance issues across the entire range of company sizes. Location: Philadelphia, PA Date: April 12th & 13th, 2018 and Time: 9:00 AM to 4:00 PM Price: Register now and save $200. (Early Bird) Contact us today! NetZealous LLC DBA GlobalCompliancePanel Registration Link - http://www.globalcompliancepanel.com/control/globalseminars/~product_id=... |
Contact Name: | NetZealous LLC DBA GlobalCompliancePanel |
Contact Email: | support@globalcompliancepanel.com |
Contact Phone: | 800-447-9407 |