Webinar on Writing Effective SOPs for Medical Device Quality Management Systems

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Category Medical Devices

Deadline: July 22, 2106 | Date: July 22, 2106

Venue/Country: Online, Canada

Updated: 2016-06-30 18:43:05 (GMT+9)

Call For Papers - CFP

Areas Covered in the Session :

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

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

Subject Matter Experts and others writing procedures

Internal Auditors and Managers

Training Specialists

CAPA Specialists

Supplier Quality Engineers and Auditors

Quality/Compliance managers or directors for Medical Device companies

General Managers wanting to learn how to understand Quality System requirements

Directors, VPs, and others attending management review