International Summit on
GMP,GCP,QA,QC and Validation
December 3-5, 2012 DoubleTree by Hilton Philadelphia Center City, USA
OMICS ABOUT OPEN ACCESS CONFERENCES JOURNALS FAQ'S BLOG CONTACT FEEDBACK
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:


 

Let us meet Again @ GMP-2013

Expert Presentations
Antonella A. Maggio

Pharmascience

Canada
Ashraf Youssef

AYPharma Safety Consulting

USA
Brett Vengroff

ComplianceLogix

USA
Charles H Pierce

Medpace

USA
Cheryl D Spencer

CQMS

Canada
Chitra Edwin

University of Cincinnati

USA
Christopher Joseph Devine

Devine Guidance International

USA
Cynthia Juncosa

Lean compliance Partners
USA
Elizabeth N De Gaspar

Sao Paulo SP

Brazil
Ellen Leinfuss

UL EduNeering

USA
Fernandos G

Development Team Consulting

Spain
Igho Onakpoya

University of Oxford

UK
J. Lawrence Stevens

One Way Consultants

USA
James Carron

Flatirons Pharmaceuticals

USA
James R Bruno

CAP Solutions

USA
Jerry xu

WuXi AppTec

China
Joeh Biehl

Propharma

USA
Julie Blasingim

Schulman Associates IRB

USA
Kaitlin Bratlie

Iowa state university

USA
Kosta Makrodimitris

Advisor

USA
Linda Biava

Regulatory Compliance Associates

USA
Margery Ross

Development QA Biologics Early Phase GMP

USA
Moe Alsumidaie

Chief Scientific Officer of Annex Clinical

USA
Myriam Ochart

O-CHART Management Consultants

USA
Nayaz Ahmed

PrimaPharm

Inc USA
Patricia Santos Serrao

MasterControl Inc

USA
Philip Onigman

Independent Bio Technology Consultant

USA
Pierrette J Oge-Cazeau

Palm beach State College

USA
Ram Balani

FDASmart Inc

USA
Ravi Samavedam

Bio SEQ

USA
Robert Beall

Propharma

USA
W. Parker Nolen

Indiana University Office of Research Administration

USA
Walid Sellem

Eli Lilly Company

France
Follow us on
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
Toll free: 1-800-216-6499(USA & Canada),
1-800-651-097(Australia), 0805-080048(Europe)
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