on
2nd International Summit on GMP, GCP & Quality Control
November 12-14, 2013 DoubleTree by Hilton Hotel Chicago-North Shore USA
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GMP-2013 Report

2nd International Summit on GMP, GCP & Quality Control was successfully held on November 12-14, 2013, DoubleTree by Hilton Hotel Chicago - North Shore Conference Center, USA, with a theme "Ensuring the Quality standards of Manufacturing process" which tracked the evolution in manufacturing and quality guidelines. GMP-2013 brought together the International blend of people from pharmaceutical, biotech & medical devices companies, business entrepreneurs, pharmaceutical consultants, leading universities and research institutions making it the largest endeavor from OMICS Group. All the papers presented at this conference were published in special issue of Journal of Developing Drugs: Open Access.

GMP-2013 opened up new vistas and fostered collaborations in the industry and academia.

The conference was embarked with an opening ceremony followed by a series of lectures delivered by both Honorable Guests and members of the Keynote forum. The adepts who promulgated the theme with their exquisite talk were;

Ashraf Youssef, AYPharma Safety Consulting, LLC., USA

Gerard Pearce, SQA Services, Inc., USA

Myriam Ochart, Lean Compliance Partners, USA

James Huang, Forest Laboratories, Inc., USA

Patricia Henley, London School of Hygiene & Tropical Medicine, UK

Workshop: A workshop on “Zippy Lean Workshop (Production Line Simulation)” conducted by Myriam Ochart, Lean Compliance Partners, USA & Jennifer Leny, American Society for Quality, USA.

Workshop: A workshop on “Highlights of Process Analytical Technology (PAT) & FDA Directives” conducted by Shib Mookherjea, ValQual International, USA.

OMICS Group has taken the privilege of felicitating GMP -2013 Organizing Committee, Keynote Speakers and business delegates who supported for the success of this event.

OMICS Group, on behalf of the conference, congratulates the Best Poster awardees for their outstanding performance in the field of Pharma regulatory affairs and appreciates all the participants who put their efforts in poster presentations and sincerely wishes them success in future endeavors. Our warm gratitude to our sponsors, exhibitors & media partners for associating with the conference.

Following on the heels of this successful event we are excited to announce 3rd International Summit on GMP, GCP & Quality Control Slated on September 25-26, 2014, at Valencia Convention Center, Spain, with a theme Manufacturing and Quality Guidelines; Training and Beyond” and wish that with your overwhelming support for GMP Summit -2014 will become an outstanding event.



Expert Presentations
Gerard Pearce

SQA Services, Inc.,

USA
Ashraf Youssef

AYPharma Safety Consulting

USA
Patricia Henley

London School of Hygiene & Tropical Medicine

UK
James Huang

James Huang Forest Laboratories, Inc.,

USA
Jacqueline McCulloch

Clarkston Consulting

USA
Jason Ruckert

Advanced Testing Laboratory

USA
Lucy H H Parker

St George├óÔé¼Ôäós Healthcare NHS Trust

UK
Abitha Sundararajan

Med Manage Systems

USA
Brigitte von Rechenberg

University of Zurich

Switzerland
M.S. Lourdes Sanchez

Sintenovo SA de CV

Mexico
Naveen Kumar Venkatesham

Laurus Labs Private Limited

India
Constance E. Curts

FDA and EU Regulatory Validation Consultant

USA
Mohammad Iqbal Hossain

Novartis Ltd.

Bangladesh
Brian Hill

Brian Hill & Associates

USA
Elizabeth Rivera

STERIS Corporation

USA
Pejman Parhami

Hyland├óÔé¼Ôäós, Inc.,

USA
Jennifer Leny

American Society for Quality

USA
Shib Mookherjea

ValQual International

USA
Heather Schwalje

Emerson Life Sciences Industry Solutions Group

USA
Myriam Ochart

Lean Compliance Partners

USA
Anthony Grilli

Focus Scientifi c Solutions

USA
Mohanad A. Al-Bayati

University of Baghdad

Iraq
Peter Odeh

SNBL Clinical Pharmacology Center

USA
Conference Secretariat: GMP-2013, Conference Series Conferences
47 Churchfield Road, London, W3 6AY, UK,
Tel: +44-800-014-8923 , Fax: +44-203-004-1517
Toll free: 1-800-216-6499(USA & Canada),
1-800-651-097(Australia), 0805-080048(Europe)
Operated by: Editors - Journal of Developing Drugs, Advances in Pharmacoepidemiology & Drug Safety and Pharmaceutica Analytica Acta
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