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Supplier Audit

The Basics of Conducting a Supplier Audit – Webcast On-Demand


In this 51-minute webcast, Danielle DeLucy, Subject Matter Expert in the areas of quality assurance and quality systems, shows how to effectively conduct a supplier audit.

Your Webcast Content Package includes

  • 51-minute webcast audio presentation
  • 46-slide powerpoint presentation
    • Audit Report with GMP Questionnaire Template – This comprehensive 78-page PDF document is broken down into the following categories, including: executive summary, audit scope and objectives, introduction and company overview, facility tour & review of operations and quality systems.This document includes a GMP audit checklist. It is broken down into the following categories, including: quality management, audit observations, personnel building and facilities, process equipment, documentation and records, materials management, production and process controls, packaging and Identification labeling of APIs and intermediates, storage and distribution, laboratory controls, validation, change control & CAPA, rejection and re-use of materials, complaints and recalls and more.
    • Pre-audit Questionnaire Template -This four (4) page PDF document is broken down into six categories, including: firm information, business organization, worker information, job descriptions, subcontractor/independent contractor information and contractor information categories.
    • IPEC Quality Agreement and Template – Recommended Information Resource – Download Here

Product Description

Why Should You Attend

Life science manufacturers are held responsible by FDA for the performance of their outsourced partners. There are several Food and Drug Administration regulations that apply to conducting a supplier audit, and this is one of the most cited 483 and Warning Letter citations. This webcast reviews the fundamentals from why audit a supplier to writing the audit report

Areas Covered in the Webcast

Who and what are suppliers-examples, defining a supplier audit, why perform a supplier audit, who should perform a supplier audit, how to select an audit team, audit logistics and a pre audit questionnaire-discussion and example are reviewed.

What do I audit? Questions to ask for, including:QMS, document and data control, receiving inspection, inventory management, process control, corrective action, personnel training, and plants and grounds

Using audit checklists – Internal Quality Management System Checklist Audit (ISO 9001:2000), during the audit: guidelines, closing out the audit, audit report, grading the supplier/supplier scorecard example/discussion, audit scoring-pros and cons, quality agreements

Case scenario-responsibility for data integrity in laboratory records and test results

Who Will Benefit

Industry professionals from many areas who may interact directly with regulatory inspectors or who help prepare for inspections, including:

  • Quality Assurance/Quality Control
  • Management
  • Training
  • Regulatory
  • Technical Operations
  • Manufacturing

For Customer Care and Group Discounts – Please Contact Us
Phone: (+1) 844.686.5750

Video Excerpts– See complimentary excerpts from the webcast

Closing Out the Supplier Audit

Supplier Audit Logistics The Pre-Audit Discussion

Instructor Profile

Danielle DeLucy is an industry veteran and specializes in the areas of Quality Assurance and Quality Systems as a consultant. Prior to this role, Danielle has been in the industry for 15 years serving in numerous quality management roles, such as the Director of Product Quality with oversight of sterility assurance practices and numerous filling and packaging operations. Danielle began her career as a Quality Control pharmaceutical microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the quality management arena with increasing responsibility. She has helped to lead many regulatory health inspections and was instrumental in the coaching process of her peers prior to any inspection. Currently, Danielle assists companies who: 1) are faced with warning letters and consent decrees; 2) wish to improve GxP practices; and 3) need to establish more robust quality systems.

Refund Policy – Courses and Webcasts

Registrants may cancel up to two working days prior to an on-line course or webinar start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. On-site training can be cancelled up to ten business days prior to training. Windshire will be compensated for any travel cancellation fees. Courses and webinars may be cancelled due to unavoidable factors. Registrants will be notified if a cancellation occurs. Attendees can choose between the recorded (on-demand) version of the webinar or a full refund for any Windshire cancelled webcast.

We encourage feedback from our clients. To contact us, please email or call (+1) 844.686.5750.


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