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

Webinar on Implementing an Internal Audit Program of QMA, Persisting to ISO 13485 & 21 CFR Part 820

 
Seminar - Online
 
This webinar is intended to help you adequately develop an internal audit program of a firm's quality management system (QMS) as required by ISO 13485 or 21 CFR Part 820.
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Tags: Medical Device Technology, March, Webinar, Quality Control, 2015, Seminar

Webinar On Quality Auditing for Added Value and Continuous Improvement

 
Seminar - Online
 
This presentation will cover basic auditing principles to enhance your own internal audit program to add real value to the organization.
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Tags: March, Webinar, Quality Control, 2015, Healthcare Quality, Seminar

2-day In-person Seminar on Validation & Part 11/Annex11 Compliance of Computerized Analytical Systems & Data

 
Seminar - Singapore
 
This 2-day course provides the regulatory background and guides attendees through the complete equipment qualification, calibration and computer system validation processes from planning to report.
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Tags: 2014, November, Laboratories, Singapore, Quality Control, Seminar

GMP Compliance for Pharmaceutical Quality Control Laboratories in Hong Kong

 

Conference - Hong Kong

This course is designed for people who are growing in their knowledge of pharmaceutical quality control practices and regulations.

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Tags: 2014, Laboratories, September, Quality Control, pharmaceutical, Hong Kong, Conference

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

Seminar on GMP Compliance for Pharmaceutical Quality Control Laboratories in Melbourne

 

Seminar - Melbourne, Australia

This course is designed for people who are growing in their knowledge of pharmaceutical quality control practices and regulations.

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Tags: 2014, Laboratories, Medicine, September, Quality Control, pharmaceutical, Australia, Melbourne, Seminar, Life Sciences

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

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