The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: April 18, 2019 from 10am to 11am
Street: 161 Mission Falls Lane, Suite 216,
Website or Map: https://www.compliance4all.co…
Phone: Event Manager
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Feb 21, 2019
Life science manufacturing plants have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.
Why should you Attend:
If your design and manufacturing resources are spending too much time on documentation and not enough time on actual design and manufacturing you as a manager need to be looking for ways to simplify their work.
Areas Covered in the Session:
Basic functions found in a life sciences manufacturing plant
Key types of controlled documents and records for manufacturing
Quality Management System (QMS) elements controlled via documentation
Bringing it all together
Who Will Benefit:
Jose Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems.
Event Fee: One Dial-in One Attendee Price: US $150.00
Compliance4All DBA NetZealous,