ComplianceOnline

Supplier Quality Management (SQM) for Pharma

Instructor: Ronald Torlini
Product ID: 705743
Training Level: Beginner to Intermediate
  • Duration: 60 Min
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Read Frequently Asked Questions

This SQM webinar will discuss how to establish a Supplier Quality Management program from selection to approval, the ON-going maintenance and disqualification of suppliers will be explored through definition of supplier classifications. How to build risk management into the process will be discussed. The webinar will explore the use of Quality Agreements to manage suppliers.

Why Should You Attend:

SQM is one of the major Quality Systems within the pharmaceutical industry and Quality organizations. How a company manages their suppliers helps define a compliance oversight of each supplier.

Various regulatory agencies make an assessment of the SQM program which allows for the company to use the raw materials, excipients and APIs for their products.How the company manages each supplier from identification to approval is critical for a safe and effective drug product.

This webinar will help attendees experience how an SQM program is established and managed by the Quality organization and its synergy with the Supply Chain group.They will learn how suppliers are identified and when a due diligence audit is needed.The approval process is explored and on-going maintenance of the supplier and disqualification will be discussed.

The webinar will begin to discuss the use of Quality Agreements which should be one of the end results of managing suppliers.

Areas Covered in the Webinar:

  • Selection and Due Diligence
  • Audits
  • Assignment of Risk
  • Classifications of Conditional/Approved/Certification
  • On-going Maintenance
  • Disqualification
  • Quality Agreements

Who Will Benefit:

  • Quality Managers
  • Compliance Group
  • Auditors
  • Supply Chain
Instructor Profile:
Ronald Torlini

Ronald Torlini
Principal Consultant, RP Torlini Consulting LLC

Ron Torlini of RP Torlini Consulting has over 30 years of pharmaceutical experience in SQM, CQM, systems, compliance and regulatory areas. He has worked for such companies as Sterling Drug, Sandoz, DuPont Merck, J&J and others.

His experience has been hands-on at site level and establishing corporate policy at the corporate levels.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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