The audit team communication webinar will teach you best practices for using technology–especially when conducting remote audits.
What you will learn in the Audit Team Communication Webinar
- Requirements for audit team communication as defined in ISO 19011:2018
- How, what and when to communicate with auditees, guides and observers during an audit
- Responsibilities of audit team members with regard to audit team communication
- Responsibilities of the lead auditor with regard to audit team communication
- Audit team meetings during an audit
- Sharing audit trails with other audit team members
- Best practices in using modern hardware and software technology to improve audit team communication
- Important considerations for remote audits
Who should attend the Opening Meetings Webinar?
- Lead auditors,
- Audit team members,
- Senior management,
- Supplier Quality,
- Purchasing, and
- Quality Assurance.
Other Resources
You may also be interested in our procedure for Quality Audits (SYS-021). That procedure includes the following documents:
- Quality Audits (SYS-021)
- Audit Log (LST-007)
- Supplier-Internal Audit Report Template (TMP-003)
What you will receive when you register for this webinar
- Native slide deck
- Login information for live webinar (up until June 3, 2020)
- Access to recording after live webinar
To register for this webinar, please fill in the form below.
There are four other new live webinars planned on related topics:
- Opening Meetings Webinar (free) – May 14, 2020
- How to qualify your suppliers webinar (pre-order by June 1) – June 25, 2020
- Remote auditing techniques webinar (pre-order by July 1) – July 16, 2020
- Interviews with MDSAP auditing organizations (free) – August 6, 2020
Anyone that watches all 5 webinars planned for May 14 – August 6, 2020, and reads our new book (released on Amazon in August 2020) will receive a certificate for “Remote Auditing Certification” as a thank you for your loyalty and hard work. We will include the information you need for submitting continuing education credits to ASQ, RAPs, etc. My friend John M. gave me that idea back in 2012, and that is why “Academy” is in our name.
About Your 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 802.281.4381 or by email. You can also follow him on YouTube, LinkedIn, or Twitter.