Webinar - Online
This 60-minute webinar will show how you can design a robust microbiological audit program for pharmaceutical and biopharmaceutical product manufacturing, that effectively assesses your facility and that of your supplier to ensure your facilities and products are free from microbial contamination.
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August,
Webinar,
Quality Control,
pharmaceutical,
biopharmaceutical,
2016
Course - Barcelona, Spain
Turning to efficient, flexible & continuous processing within sustainable quality
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November,
Pharmacology,
Quality Control,
Barcelona,
Spain,
2015,
Life Sciences,
biotech,
Pharma
Seminar - Online
This webinar will discuss the most important issues that apply to sterile products in order to provide an overview for attendees to evaluate their own processes and procedures.
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August,
Webinar,
Quality Control,
2015,
Seminar,
Biologics
Seminar - Online
The success of an audit by federal regulators does not always depend on the level of training provided to staff and department employees, but also in understanding the focus of recent inspections within the industry.
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July,
Webinar,
Quality Control,
2015,
Seminar
Seminar - Online
This webinar provides an overview of the Quality Management System requirements. We will discuss ISO Quality Management standards and the FDA Quality System requirements.
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Tags:
Medical Device Technology,
July,
Webinar,
Quality Control,
2015,
Seminar
Many laboratories are unsure about which QC practices are needed to assess media performance to meet not only their requirements, but also the requirements of ISO/IEC 17025: 2005.
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July,
Webinar,
Quality Control,
pharmaceutical,
2015,
Life Sciences
Seminar - Online
The webinar clarifies the regulatory concern that FDA has and whether subjecting Laboratory Developed Tests (LDTs) to FDA's device Quality System Regulation can make a measurable difference in the safety and effectiveness (reliability) of special IVDs.
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June,
Webinar,
Quality Control,
Health Care,
2015,
Seminar,
laboratory,
Biologics
Seminar - Online
Developing a Quality Management System (QMS) as a prerequisite for getting accredited is relatively easy. Maintaining the QMS to retain your accreditation status is the real challenge and a measure of the robustness your System.
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June,
Webinar,
Quality Control,
2015,
Seminar,
laboratory,
Biologics
Seminar - Online
This presentation is intended to help you get familiar with best practices for quality risk management (QRM) applicable to pharmaceutical industry (drugs, biosimilars, and biologics) as well as medical device industry.
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Tags:
Medical Device Technology,
Webinar,
May,
Quality Control,
pharmaceutical,
2015,
Seminar,
Biologics
Seminar - Online
HACCP Hazard Analysis and Critical Control Points is a management system in which product safety is addressed through the analysis and control of biological, chemical, and physical hazards from raw material production, procurement and handling, to manufacturing, distribution and consumption of the finished product.
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Tags:
Webinar,
May,
Quality Control,
2015,
Seminar,
Biologics