Seminar - Online
The secret to effective compliance documentation and technical training lies in how the analysis is conducted and how training and compliance documentation are developed as a result of that analysis.
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August,
Webinar,
2015,
Seminar,
Biologics
Seminar - Online
The area of pediatric development is relatively new and changing following the new laws. The use of adult data to support the pediatric initiative allows good adult information to support the children.
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August,
Webinar,
Pediatrics,
2015,
Seminar,
Drug Development,
Biologics
Seminar - Online
This course teaches any employee the Lean Six Sigma philosophy and how to apply it in their job on a day-to-day basis.
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July,
Webinar,
2015,
Seminar,
Biologics
Seminar - Online
Lack of use of any effective tool can often be linked to lack of understanding of the tool, the benefits of the use of the tool and how to implement the tool.
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July,
Webinar,
2015,
Seminar,
Biologics
Seminar - Online
The most common method for a customer to communicate quality requirements to a supplier is through the use of a capability index.
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July,
Webinar,
2015,
Seminar,
Biologics
Conference - Boston, MA, United States
Once you have established biologic efficacy and safety in early clinical material, your companys real challenges are only beginning.
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Tags:
Biochemistry,
United States,
October,
2015,
Boston,
Conference,
MA,
Biologics
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
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
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
Within the Pharmaceutical Industry, the changeover from one product to another on a filling/packaging line, although relatively a simple concept, has significant implications from a regulatory standpoint if cross-contamination is permitted to occur.
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July,
Webinar,
pharmaceutical,
2015,
Seminar,
1 day only,
Biologics