Controlled Document System for a Life Sciences Manufacturing Plant

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Category Life Sciences Manufacturing, Lean Documents Trainings, QMS, fda quality management system, clinical laboratory compliance, clinical data management compliance, clinical importance of compliance

Deadline: April 16, 2019 | Date: April 18, 2019

Venue/Country: Online, U.S.A

Updated: 2019-02-18 15:33:48 (GMT+9)

Call For Papers - CFP

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:

Manufacturing Engineering

Design Assurance

Quality Assurance

Operations

Document Contro

Speaker Profile:

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

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com