Science Researcher Update: Spotlight on Meetings, Conferences, and Events

Webinar on Managing Product & Process Risk through Failure Mode & Effects Analysis (FMEA)

 
Seminar - Online
 
Conducted early in the process development cycle, the Failure Modes and Effects Analysis tool is used to identify risks and then adjust the manufacturing or service process to reduce the identified risks and improve quality.
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Tags: April, Webinar, Quality Control, 2015, Seminar, Biologics

Webinar on Drug Development & Discovery by FDA Standards

 
Seminar - Online
 
This webinar will lay out the whole process systematically and in a simplified manner.
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Tags: Medical Device Technology, Drug Discovery, Canada, April, Webinar, 2015, Seminar, Drug Development, Biologics

Webinar on Transfer of Analytical Methods & Procedures according to USP 1224

 
Seminar - Mississauga, Ontario, Canada
 
This seminar will give a good understanding of USP and FDA requirements and provide recommendations and tools for effective implementation.
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Tags: Canada, April, Webinar, 2015, Seminar, Biologics

Webinar on Current Good Manufacturing Practices (cGMP) for Medical Devices & IVDs

 
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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Tags: Medical Device Technology, Canada, April, Webinar, Quality Control, 2015, Seminar

Webinar on Method Validation: Utilizing Quality by Design (QbD) & Risk in Implementation

 
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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Tags: Canada, April, Webinar, Quality Control, pharmaceutical, 2015, Seminar, Biologics

Webinar on 2015 HIPAA Changes

 
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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Tags: Canada, April, Healthcare, Webinar, Pharmaceuticals, 2015, Seminar

Webinar on 21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents & Lean Configuration

 
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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Tags: Medical Device Technology, Canada, April, Webinar, Quality Control, 2015, Seminar

Webinar on FDA Regulation of Mobile Apps

 
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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Tags: Medical Device Technology, Canada, April, Healthcare, Webinar, 2015, Seminar, Biologics

Webinar on Laboratory Accreditation: Getting there is Just the Beginning

 
Seminar - Mississauga, Ontario, Canada
 
Why do you want to become accredited? Where do you start?
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Tags: Canada, April, Webinar, Quality Control, 2015, Seminar, laboratory, Biologics

Webinar on Big Data in FDA-Regulated Industry: Best Practices for Systematic Use

 
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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Tags: Medical Device Technology, food science, April, Webinar, 2015, Seminar, Biologics

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