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Pharmaceutical Manufacturing

Zoom in  Zoom out Publish date: 2014-03-13   Hits: 105   Status: Status
Date 2014-04-23 to 2014-04-23
City Michigan
Address 201,N Squirrel road, Suite 1007, Auburn Hills, Michigan United States - 48326.
Exhibition hall on line
Sponsor John Gordan

Event Description

The FDA and its European counterpart, EMA, require drug manufacturers to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate compliance and state of control. This program provides the foundation for an efficient and effective batch record review process and provides pharmaceutical companies with two strategies. First, the key to recognizing what your firm needs to demonstrate control of your manufacturing operations. And, secondly, how to put into place a proactive training regime and batch record review management system.

quality assurance batch record reviewers

production personnel who are responsible for batch record reviews

QA managers and supervisors of batch record reviewers

Online Regulatory Compliance Training, Compliance Training, regulatory compliance training, Online compliance Training, e-learning, Regulatory standards Guidelines, Best Practices, Regulatory Compliance, Compliance Management, Corporate Compliance, Compliance Solutions, FDA and ISO regulations, Process and Design Validation, Online Compliance, Global Compliance, Medical Devices Directive, ISO Compliance, ISO14971, ISO 14971:2007, Global Compliance Trainings, Online Training, Online Trainings

Live Session for one participant

Price: $225.00


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Corporate Live Session 4 to 10 participants in single location.



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Recorded Session Access recorded sessions only for one participant unlimited viewing for 6 months.

Price: $275.00



Contact information
Contact: webinar@globalcompliancetraini
Tel: +1-248-212-0588
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