Conference - Toronto, Canada
Today, biospecimen collections are used by multiple research groups for varying research aims, from basic research through clinical trials.
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Tags:
Biotechnology Current Events,
Canada,
Congress,
July,
2015,
Toronto,
biobanking,
Conference,
Biotechnology,
Life Science
Seminar - Online
The Theory of Lean Documents is the product of applying lean principles to the Quality Management System (QMS) documents typically found in regulated industries.
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July,
Webinar,
pharmaceutical,
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 seminar (webinar) is intended to help those in pharmaceutical and medical device industry involved in interacting and communicating with the health authorities.
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July,
Webinar,
2015,
Seminar,
Biologics
Webinar - Online
Size exclusion chromatography (SEC) is one of the key methods used in the characterization of biopharmaceuticals, such as monoclonal antibodies (mAbs).
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Tags:
genetic engineering,
July,
Webinar,
Protein,
biopharmaceutical,
2015,
Biotechnology
Seminar - Online
Recently the FDA has released a new comprehensive guidance for validation of analytical methods.
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July,
Webinar,
2015,
Seminar,
Biologics
Manufacturers and importers must report adverse events associated with a risk to health or death. Until now, the reports were submitted in hardcopy using MedWatch form 3500A.
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Tags:
Medical Device Technology,
July,
Webinar,
2015,
Seminar
Seminar - Princeton, NJ, United States
The goal of this seminar is to familiarize senior executives and high level managers from every department in a regulated firm, with their personal responsibility in assuring your firm of the highest level of FDA Compliance.
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July,
Webinar,
Development,
Princeton,
NJ,
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
This webinar will be addressing OSHA and the medical practice. It will address risk factors in terms of an OSHA audit, blood borne pathogens, and HAZCOM, universal precautions, etc.
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Tags:
July,
Healthcare,
Webinar,
2015,
Seminar