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Site language : English - Français
Ref : 29041
Event :Controlled Document System for a Life Sciences Manufacturing Plant

Date :Thursday April 18th, 2019

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


Further information

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 
Bringing it all together
Who Will Benefit:
Manufacturing Engineering
Design Assurance
Quality Assurance
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

Further information

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Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All [...]

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Presentation sheet from Compliance4All


Controlled Document System for a Life Sciences Manufacturing Plant Pharmacy - Medicine - Bio-Technologies - Public Health
education, drug development, conference, fda regulations, global trainings, health
Everyone, Design Assurance Quality Assurance Operations Document Control
50 1 --


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