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

15th Annual BioResearch Product Faire™ Event at University of Michigan, Ann Arbor

 
BioResearch Product Faire Event - Ann Arbor, MI, United States
 
The 15th Annual BioResearch Product Faire™ Event at University of Michigan, Ann Arbor, is a networking and idea generation event and will include new product demonstrations, supplier exhibits, and relevant topic seminars.
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Tags: University of Michigan, Biotechnology Calendar, University of Michigan Ann Arbor, July, United States, 2015, Ann Arbor, BioResearch Product Faire Event, Life Sciences, Biotechnology, MI

5th Annual BioResearch Product Faire™ Event at Michigan State University, East Lansing

 
BioResearch Product Faire Event - East Lansing, MI, United States
 
The 15th Annual BioResearch Product Faire™ Event at Michigan State University, East Lansing, is a networking and idea generation event and will include new product demonstrations, supplier exhibits, and relevant topic seminars.
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Tags: Michigan State University, Biotechnology Current Events, July, United States, 2015, BioResearch Product Faire Event, Life Sciences, Biotechnology, MI, East Lansing

How to Achieve Adherence to Standard Operation Procedures (SOP)

 

Webinar - Online

Describe the North America Commercial Nuclear successful method used method greater than twenty years and how it is applied in any industry using SOP (controlled and regulated) documents to describe instructions to complete work tasks.

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Tags: 2014, Michigan, United States, Webinar, May, Quality Control, pharmaceutical, Life Sciences, Conference, MI

Webinar on Risk Analysis Tools by Global Compliance Trainings

 

Webinar - Online

The ISO 12971 standard on risk management for medical devices describes risk analysis tools such as PHA, FTA, FMEA, HAZOP, and HACCP but does not provide the depth needed to use the tools correctly.

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Tags: 2014, Medical Device Technology, Michigan, United States, Webinar, May, Quality Control, pharmaceutical, Life Sciences, Conference, MI

Webinar on FDA Inspection: Preparation and Management

 

Webinar - Online

This webinar is intended to help you get familiar with how to prepare for and manage an FDA inspection.

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Tags: 2014, Michigan, United States, Webinar, May, Quality Control, Life Sciences, Conference, MI

Preventing Medical Device Recalls - Global Compliance Trainings' Webinar

 

Conference

Preventing device recalls requires thoroughly predicting what can go wrong proactively using the risk analysis tools. Then it requires revising the specification to accommodate the mitigations for the identified failure modes and harm scenarios.

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Tags: 2014, Medical Device Technology, Michigan, United States, Healthcare, Webinar, May, Quality Control, Life Sciences, Conference, MI

Implementing a Quality Management System for Medical Devices & In Vitro Diagnostics

 

Webinar - Online

This webinar is intended to help you get familiar with US quality system regulations and how to implement an FDA-compliant quality management system for medical devices including in vitro diagnostic medical devices (IVDs).

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Tags: 2014, Medical Device Technology, Michigan, United States, Webinar, May, Quality Control, Life Sciences, Conference, MI

Writing Good Device Specifications - Recorded Webinar

 

Webinar - Online

Product recalls in 2013 were 28% higher than 2012, and are historically at the highest level. The number one cause is the poor and incomplete specifications.

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Tags: 2014, Michigan, United States, Webinar, May, Quality Control, Life Sciences, Conference, MI

FDA & Overview of ISO 13485 - Global Compliance Trainings' Webinar

 

Webinar - Online

This webinar is intended to help you get familiar with FDA’s implementation of statutory requirements for setting risk-based FDA inspectional priorities.

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Tags: 2014, Michigan, United States, Webinar, May, Quality Control, Life Sciences, Conference, MI

US FDA 510(k): How to Put Together a Compelling 510(k): Good Practices with Increased Awareness

 

Webinar - Online

This webinar is intended to demonstrate how to put together a compelling (bullet proof) 510(k) in compliance with the FDA’s eCopy and RTA policy so that your time, energy and financial resources can be effectively used to expedite your 510(k) clearance, potentially leading to saving millions.

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Tags: 2014, Michigan, United States, Webinar, May, Quality Control, Life Sciences, Conference, MI

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