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International Summit on
GMP,GCP,QA,QC and Validation
December 3-5, 2012 DoubleTree by Hilton Philadelphia Center City, USA
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GMP,GCP & QA,QC Validation 2012
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GMP,GCP & QA,QC Validation 2012 Report
OMICS Groups International Conference on GMP, GCP, QA, QC & Validation was completed successfully on December 3-5, 2012 at Philadelphia, USA. A very generous response and active participation from the Editorial Board Members of OMICS Group Journals, pharmaceutical industry professionals, and decisions makers from the field of manufacturing quality made the conference an immensely productive event for the attendees.
A well organized B2B between the attendees and the Exhibitors like Qumas, Master Control, and Apollidon turned out to be the prime feature of the conference.
An industry oriented approach of the conference focused on the topics like Current GMP Guidelines for Pharmaceuticals, Current Regulations and Quality Standards, GLP, GCP, and cGMP, Technology Transfer for Industrial pharmaceuticals, Quality Management and Quality Improvement in Research, paving the path of many new strategies for maintaining the manufacturing Quality of the products.
The conference was initiated with the lectures on Honorable Guests followed by keynote forum. Professionals from various organizations across the globe rendered their expertise and enjoyed the event.
Exhibitions:
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Expert Presentations
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Conference Secretariat: GMP & GCP-2012, OMICS Group Conferences
5716 Corsa Ave, Suite 110, Westlake, Los Angeles, CA 91362-7354, USA
Tel: +1-650-268-9744, Fax: +1-650-618-1414
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Toll free: 1-800-216-6499(USA & Canada), 1-800-651-097(Australia), 0805-080048(Europe)
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Operated by: Editors - Clinical & Experimental Pharmacology and Clinical Pharmacology & Biopharmaceutics, Journal of Clinical Research & Bioethics |
The Organizers reserve the rights to make changes and adjustment to the information in this website
© Copyright 2008-2012 OMICS Group - All rights reserved |
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