Tool kit for supplier auditing – Forms, templates, etc.

This supplier auditing tool kit consists of forms and templates for use during the preparation and execution of supplier audits.

What’s included in the supplier auditing tool kit?

1. supplier auditing report template
2. template for taking notes during an audit
3. template for clause traceability tracking
4. template for a supplier audit agenda
5. turtle diagrams for each of the processes identified in the supplier audit agenda

Supplier auditing webinar and took kit bundle – 299.00

Webinar, Supplier Auditing Tool Kit and Exam Bundle

Planning Annual Audit Schedule Webinar; Supplier Auditing Tool Kit and Audit Planning Exam Bundle includes: 1) native slide deck, 2) recording of webinar, 3) supplier auditing report template, 4) template for taking notes during an audit, 5) template for clause traceability tracking, 6) template for a supplier audit agenda, 7) turtle diagrams for each of the processes identified in the supplier audit agenda, and 8) an exam specific to planning audit schedules.

Price: $299.00

Please note: The supplier audit tool kit will be delivered to the email address provided in the shopping cart transaction. After the transaction is verified, please check your email for the download of a zip file containing the five documents. The tool kit includes the above templates, a recording of the webinar presentation, the native PowerPoint slide deck, and an exam to verify training effectiveness.

Supplier quality management resources to supplement our tool kit

Our supplier auditing tool kit will help you prepare for your next supplier audit, but before you audit a supplier you will need to gather other supplier qualification information. Our supplier quality management procedure is SYS-011, or you might also be interested in our webinar on Remote Auditing and Supplier Auditing. We also provide supplier auditing services if you need to outsource some of your supplier audits.

About  the  Instructor

Rob Packard is a regulatory consultant with ~25 years of experience in the medical device, pharmaceutical, and biotechnology industries. He is a graduate of UConn in Chemical Engineering. Rob was a senior manager at several medical device companies—including the President/CEO of a laparoscopic imaging company. His Quality Management System expertise covers all aspects of developing, training, implementing, and maintaining ISO 13485 and ISO 14971 certifications. From 2009 to 2012, he was a lead auditor and instructor for one of the largest Notified Bodies. Rob’s specialty is regulatory submissions for high-risk medical devices, such as implants and drug/device combination products for CE marking applications, Canadian medical device applications, and 510(k) submissions. The most favorite part of his job is training others. He can be reached via phone at +1.802.258.1881 or by email. You can also follow him on YouTube, LinkedIn, or Twitter.