Seminar - Boston, MA, United States
In the face of aggressive audits by regulatory agencies, life sciences companies continue to face unprecedented compliance challenges in ensuring data integrity.
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Seminar - Morton Grove, IL, United States
Regis Technologies invites you for a seminar on FDA 505(b)(2) applications.
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Tags: March, United States, Seminar, IL, 2016
Conference - Galveston, TX, United States
In 2016 we will focus on the question: what would it take for the emerging generation of researchers to go from a collage of individual achievements to a real breakthrough in understanding life's origins – presently one of the greatest mysteries of science?
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Tags: Biology, Chemistry, Earth, January, Seminar, Life Science, 2016
Seminar - Boston, MA, United States
Cardiovascular Seminar Series Speaker: Cecilia Wen Ya Lo, PhD F. Sargent Cheever Chair, Professor and Chair of the Dept of Developmental Biology University of Pittsburgh School of Medicine
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Tags: research mice, cardiovascular research, heart disease, United States, December, Genetic, 2015, Boston, Seminar, MA, Mice
Seminar - Virtual
The successful filing of an Investigational New Drug application (IND) is a pivotal milestone for an emerging pharma company.
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Tags: Healthcare, Webinar, pharmaceutical, December, 2015, Seminar, biotech, Pharma
Seminar - Morton Grove, IL, United States
Wave after wave of quality initiatives have come from other industries and failed to take root.
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Tags: November, United States, 2015, Seminar, IL
Seminar - Online
This seminar will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.
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Seminar - Online
This seminar will give you current excellent understanding of how FDA is working today and how assure your quality systems will meet FDA expectations.
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Tags: United States, September, Webinar, Princeton, NJ, 2015, Seminar, Genetics, Biotechnology
Seminar - Online
Understanding the regulatory requirements set out under good laboratory practice (GLP) regulations is important so that the GLP requirements can be adequately implemented, helping to streamline regulatory processes and to save a significant time and effort during the process.
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Tags: September, Webinar, 2015, Seminar, laboratory
Seminar - Online
This training program is essential for those introducing lean principles at the company’s earliest stages. A startup plant faces many challenges and options.
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Tags: Medical Device Technology, August, Webinar, 2015, Seminar
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