Developing Supplier Quality Auditor Training Programs
September 21, 2010(Ended)
Online Webinar
In this webinar our expert trainer Jeff Kasoff will explain the best way to identify which employees can be the most effective auditors and how to train them.Why You Should Attend:
In order to assure your company is in substantial compliance, you must have an audit team that is trained to identify noncompliances present in both your quality system and that of your suppliers. This session shows you the most efective way to identify those employees who will be the most effective auditors, and how to train them to accurately assess the compliance status of your company and suppliers. Also covered will be the responsibilities of each position on the audit team, as well as the audit process, including several supplier-specific implications. Inadequate performance of your audit team can have serious adverse effects in the form of both product and regulatory impications.
Areas Covered in the Seminar:
- Importance of the Audit Team Coordinator.
- Auditor Selection.
- Auditor Training Requirements.
- Auditor Responsibilities.
- Audit Planning.
- Pre-audit Preparation.
- Audit Performance.
- Post-audit Requirements and Tasks.
This webinar will provide valuable assistance to all companies that are subject to FDA regulations, in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:
- Top management
- Regulatory/quality management
- Internal auditors
- Supplier auditors
- Industry personnel who wish to implement a supplier or internal audit program
Prices *
299 US Dollar
Exhibition
No exhibition
Organization
Categories
Concurrent events
- Why Medical Device Companies Receive Warning Letters - Webinar by GlobalCompliancePanel 2010
- Quality by Design (QbD) and Analytical Methods - Webinar by GlobalCompliancePanel 2010
- Auditing Computer System Validation Materials - Webinar by GlobalCompliancePanel 2010
- ComplianceOnline Webinar - Medical Device Changes and The 510(k) 2010
- What are the “Good Clinical Practices” (GCP) of Research involving Human Subjects
- EU IMPD vs. US IND: Comparing the Content and Agency Expectations
- Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs
- Project Management Certification Study Group - Information Year 2010
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
Articles/News/Press releases
- Business Events Aim to Improve Every Aspect of a Business
- Business Seminars can Change your Outlook
- Chronic lymphocytic leukemia and related disorders - Clinical
- Absract : Percutaneous Nephrolithotomy(PCNL): 10 years Experience with 7200 cases, Report of Results and Complications in Southern Iran
- Corneal endothelial recovery in patients undergoing small incision cataract surgery comparison between diabetics and non diabetics.
- Estimation of Serum Leptin Levels in Patients with chronic hepatitis C (CHC)
