Seminar - Amsterdam, Netherlands
Review of the latest science and practice in organisations.
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June,
Netherlands,
Amsterdam,
2015,
Seminar,
Psychology
Seminar - Mississauga, Ontario, Canada
This webinar is intended to help you get familiar with FDA’s Quality System Regulations (cGMP) for medical devices including in vitro diagnostic medical devices.
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Medical Device Technology,
Canada,
April,
Webinar,
Quality Control,
2015,
Seminar
Seminar - Mississauga, Ontario, Canada
Pharmaceutical industry is experiencing a growing need to improve performance driven by global competition and the increasing impact of information technology.
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Canada,
April,
Webinar,
Quality Control,
pharmaceutical,
2015,
Seminar,
Biologics
Seminar - Mississauga, Ontario, Canada
This lesson will be addressing the major changes under the Omnibus Rule and any other applicable updates for 2015.
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Canada,
April,
Healthcare,
Webinar,
Pharmaceuticals,
2015,
Seminar
Seminar - Mississauga, Ontario, Canada
In this webinar, we apply the Theory of Lean documents and its corollary Theory of Lean Configuration to present a fresh approach to following 21 CFR Part 820, yet is based on solid principles and proven practices.
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Medical Device Technology,
Canada,
April,
Webinar,
Quality Control,
2015,
Seminar
Seminar - Mississauga, Ontario, Canada
The use of mobile apps as a medical device continues to mushroom. Approximately 85% of adults use cell phones.
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Medical Device Technology,
Canada,
April,
Healthcare,
Webinar,
2015,
Seminar,
Biologics
Seminar - Mississauga, Ontario, Canada
Why do you want to become accredited? Where do you start?
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Canada,
April,
Webinar,
Quality Control,
2015,
Seminar,
laboratory,
Biologics
Seminar - Mississauga, Ontario, Canada
In this 60-min presentation, the speaker will guide you through the details of how to identify and use big data for your maximum benefits applicable to FDA-regulated industry.
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Medical Device Technology,
food science,
April,
Webinar,
2015,
Seminar,
Biologics
Seminar - Mississauga, Ontario, Canada
This webinar on Design History Files (DHF) will provide a step-by-step procedure for all medical device companies that are in need of bring their product design history files up to date with the current standards.
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Medical Device Technology,
Canada,
April,
Webinar,
Quality Control,
2015,
Seminar
Seminar - Mississauga, Ontario, Canada
The seminar begins with a discussion of relevant regulatory requirements, as motivation for calculating "confidence/reliability".
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Medical Device Technology,
April,
Webinar,
2015,
Seminar