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2019 - Secrets to Writing Effective SOPs

Date2019-09-24

Deadline2019-09-24

VenueOnline, USA - United States USA - United States

KeywordsMedical Devices

Websitehttps://bit.ly/2k5ck68

Topics/Call fo Papers

OVERVIEW
Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well-written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well-written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work. This webinar will help you structure your QMS and develop accurate, clear, unambiguous SOPs.
LEARNING OBJECTIVES
FDA and NB expectations for SOPs
Lessons Learned from 483s and warning letters
Common problems with SOPs
How to structure your QMS and SOPs
How to outline and format your SOPs
WHY SHOULD YOU ATTEND
This 90-minute webinar will focus on how to write clear, concise SOPs that your employees can follow.
Understand QMS structure
Understand key elements of SOPs
Understand FDA expectations
Understand ways to make your SOPs clearer and easy to follow
Understand common problems and areas for improvement
Making your SOPs effective and efficient
AREAS COVERED
Using process maps to make procedures clear
Using diagrams and visuals
Maintaining and controlling SOPs
Ensuring adequate training to your SOPs
Best Practices
WHO WILL BENEFIT?
Quality Systems Specialists
Document Control Specialists
Quality and Compliance Specialists
Internal Auditors and Managers
Training Specialists
CAPA Specialists
Supplier Quality Engineers and Auditors
Quality/Compliance managers or directors for Medical Device companies
SPEAKER
Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with an emphasis on quality, compliance, and six sigma. She has worked at industry leading companies such as GE, J&J, and Medtronic with an extensive background in quality and compliance for medical devices, including roles as Executive Business Consultant, Worldwide Director of Product Quality, and Director of Corporate Compliance.
For more detail please click on this below link:
http://bit.ly/2k5ck68
Email: support-AT-247compliance.com
Tel: +1-(510)-868-1040

Last modified: 2019-09-09 19:47:55