Calibration in the FDA Regulated Industry
October 12 - 13, 2009
Amsterdam, The Netherlands
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Who Should Attend
This overview course is intended for individuals in all
industries, but specifically individuals in FDA regulated
industries, who are responsible for establishing, maintaining,
operating a calibration program, and auditing of calibration
activities, including:
• Quality Assurance
• Quality Control
• Quality Engineering
• Technical Support
• Research and Development
• Facilities and Equipment Maintenance
Description
The regulations covering manufacture and control of drug
products and medical devices require that firms have a
program for the calibration of test and measurement
equipment. A requirement for calibration is also defined in ISO
9000 and a Quality System for a calibration laboratory is
described in ISO 17025. Calibration is a good business and
science practice followed in all industries that require
measurements for process monitoring and control. The
program must include the elements of: calibration intervals,
scheduling, specific calibration procedures, limits of accuracy
and precision and remedial action in the event that the
instrument does not meet established requirements.
This course addresses the regulatory and business
requirements for calibration as an element of a Quality System
and how these requirements support the increasing application
of process monitoring and sophisticated laboratory
instrumentation, along with the maturing discipline of
calibration in the regulated industries. It includes a discussion
of a compliant calibration program and concludes with a
discussion of a model calibration procedure.
Other Courses of Interest
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Sep 14 2009, Burlingame, CA
Analytical Methods Validation for FDA Compliance
Nov 02 2009, Dublin, Ireland
Developing Specifications for Drug Substances (APIs) and Drug Products
Aug 24 2009, New Brunswick, NJ
Developing Specifications for Drug Substances (APIs) and Drug Products
Oct 05 2009, Amsterdam, The Netherlands
Drug Product Stability and Shelf-Life
Dec 09 2009, Burlingame, CA
Drug Product Stability and Shelf-Life
Dec 14 2009, Amsterdam, The Netherlands
Laboratory Control System
Near Infrared Spectroscopy
Dec 15 2009, Amsterdam, The Netherlands
PAT Online Process Analysis
Real World Approaches to PAT and QbD Implementation
Jul 28 2009, New Brunswick, NJ
Real World Approaches to PAT and QbD Implementation
Oct 20 2009, Frankfurt, Germany
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