The webinar covers the following key areas:

·         FDA expectations for SOPs and lessons learned from 483s and warning letters

·         Using process maps to make procedures clear, and mistake proofing concepts

·         Maintaining and controlling SOPs

LEARNING OBJECTIVES

• Overview of the regulations

• FDA expectations

• Lessons learned and common mistakes

• SOP best practices

• Preparing for an FDA audit

WHO WILL BENEFIT

• Quality Systems Specialists

• Document Control Specialists

• Quality and Compliance Specialists

• Internal Auditors and Managers

• Training Specialists

• CAPA Specialists

• Quality/Compliance managers or directors for Medical Device companies

• General Managers wanting to learn how to understand Quality System requirements

• Subject Matter Experts who write procedures

Speaker Profile:Susanne Manz is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has 30+ years of professional experience.

Use Promo Code SPRS20 and get flat 20% discount on all purchases.

To Register (or) for more details please click on this below link:

http://bit.ly/2un2gL7

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