Subcontractor auditing (cGMP/Pharma/Med device industries)

Instructor: Jan Warner
Product ID: 705063
  • Duration: 90 Min
This course will describe the basic principles and requirements for building a supplier audit program. This webinar will provide a framework on which to build your subcontractor auditing program.
Purchase option for this webinar is currently unavailable. Please contact our Customer Care for more info.

Customer Care

Fax: +1-650-362-2367

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Why Should You Attend:

Supplier and subcontractor auditing is a necessary requirement for rating the quality and service of materials and services supplied to the pharmaceutical and FDA regulated industries. The objective of supplier qualification is for the customer and supplier to work together to establish to assure consistency and high quality as demonstrated by predictable conformance to customer requirements. This course will describe the basic principles and requirements for building a supplier audit program.

This webinar will provide insight and information as how to effectively carryout audits of subcontractors used to supply raw materials, equipment and services. The goal is to:

  • Understand our supplier’s quality systems
  • Ensure the raw materials, equipment and other materials are consistent and conform to known specifications
  • Guarantee the quality of supplied materials
  • Maintain supply chain visibility
  • Determine conformance of a manufacturer's quality system with regulatory requirements

Areas Covered in the Webinar:

  • Subcontractor audits
  • Training of auditors
  • Conducting the audit
  • Rating the supplier
  • Making decisions about the quality of materials supplied

Who Will Benefit:

This webinar will provide valuable assistance to professionals working in FDA regulated industries. The employees who will benefit include:

  • Quality Assurance professionals
  • Purchasing managers
  • Manufacturers
  • Suppliers
  • Contract laboratory services
  • Regulatory professionals
Instructor Profile:
Jan Warner

Jan Warner
President, IQA Consulting Services LLC

Jan Warner is an accomplished, broad-based regulatory, quality and compliance professional with over 25 years of experience in the following products and industries: pharmaceutical, medical device, OTC and personal care, homeopathic drugs, dietary supplements and cosmetics. He has held numerous upper management responsibilities in quality assurance, compliance and quality control at companies such as Pall Corporation, Luitpold Pharmaceuticals, Axiom Pharmaceuticals, Johnson and Johnson and Nobel Biocare.

He is the owner of IQA Consulting Services; a niche provider of quality and compliance services to the FDA and similarly regulated industries. Jan has extensive experience working for Fortune 500 as well as start-up companies.

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Seminars by Ex-FDA Officials

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 [email protected] call +1-888-717-2436 (Toll Free).

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