This webinar will discuss requirements for supplier and vendor qualifications. Attendees will learn how to develop a risk management plan for monitoring of suppliers, vendors and service providers. It will also discuss how to prevent recalls and advisory notices due to provided non-conforming materials or bad services.
This webinar will help attendees understand regulatory requirements and processes for vendor and supplier selection, qualification and monitoring to ensure that these third parties are in compliance with regulations and company requirements.
Why Should You Attend:
Pharmaceuticals and medical device companies spend millions of dollars to purchase raw materials and services or outsource processes. A company’s success depends on their level of interactions with their suppliers and vendors. Noncompliant products produced by suppliers will cost millions of dollars for the company in recalls, production delays, and shortages.This webinar will help attendees understand regulatory requirements and processes for vendor and supplier selection, qualification and monitoring to ensure that these third parties are in compliance with regulations and company requirements.
Areas Covered in the Webinar:
- Supplier selection and qualification process
- Supplier risk management plan
- How to conduct a supplier qualification audit
- How to deal with critical suppliers and single source suppliers
- Supplier Corrective Action required (SCAR)
- Supplier change control and production assessment
- Quality agreement requirements
Who Will Benefit:
This webinar will provide valuable assistance to all personnel involved in qualification and management of suppliers in pharmaceuticals, biotechnology, and device companies.- Managers
- Supervisors and Associates in Quality Assurance
- Quality Control Personnel
- Compliance Professionals
- Regulatory Affair Personnel
- Manufacturing Professionals
Course Provider
Yasamin Ameri,
