GMP,GCP,QA,QC and Validation
December 3-5, 2012 DoubleTree by Hilton Philadelphia Center City, USA
Quality Control-2012
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Exhibitor
Workshop
Participants List in Academia
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University of Texas at Arlington, USA
Stanford University School of Medicine, USA
Mahidol University, Thailand
Amirkabir University of Technology, Iran
Hamdard University, India
Yeshiva University, USA
University of Macau, China
Monash University, Australia
University of Michigan, Ann Arbor
Universidade Federal do Rio de Janeiro, Brazil
University of Denver, Colorado
University of Toronto, Canada
Zagazig University, Egypt
Banaras Hindu University, India
Taipei Medical University, Taiwan
University di Messina CNISM, Italy
University of Tasmania, Australia
Huazhong University of Science and Technology, China
Sogang University, Korea
University of Edinburgh, UK
Martin-Luther-University Halle-Wittenberg, USA
Universidade de Sao Paulo, Brazil
Eve University, Turkey
University of Delhi, India
Isfahan University of Technology(IUT), Iran
Taif University, Saudi Arabia
University Medical Center, Netherlands
University of Copenhagen, Denmark
University Paris 13, France
Participants List From Business
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Cadila Pharmaceuticals, India
Chemical Works of Gedeon Richter, Hungary
3S-Pharmacological Consultation & Research GmbH, Germany
Royal Brisbane and Women's Hospital, Australia
Psoriasis and Cutaneous Inflammation Research Laboratory, USA
Alcon Laboratories Inc., USA
National Institute for Materials Science (NIMS), Japan
Grup de Recerca de Reumatologia (IRHVH), Spain
Bayer Health Care, Richmond, USA
Crown Bioscience Inc., China
Hammersmith Hospital, London
Van Drie Research LLC, USA
Dr.Reddy's labs, India
Merck Research Laboratories, USA
National Institute of Pharmaceutical Education and Research (NIPER), India
AstraZeneca R&D Boston, USA
Abbott Laboratories, USA
Hutchison MediPharma Limited, China
Sage Bionetworks, USA
Central Drug Research Institute, India
Glenmark Pharmaceuticals, India
National Institute for Interdisciplinary Science & Technology (NIIST) , India
Novartis Campus, Austria
Upcoming Conferences
International Conference on QA, QC and Validation paves path for accelerating scientific discoveries with the theme of "New challenges and opportunities in QA, QC and Validation process."
Quality Control-2012 comprised of 10 tracks and 43 sessions designed to offer comprehensive sessions that address current issues in QA, QC and Validation.
Submit your Abstract to any of the following Tracks. All related Abstracts are accepted.
Register now for the conference by choosing an appropriate package suitable to you.
Renowned Speakers
Pal Mayasandra
scientist/chemist
Food & Drug Administration, USA
Jose Zayas
Nuclear Pharmacy Services, USA
Linda Biava
Regulatory Compliance Associates
Kenosha., USA
Myriam Ochart
O-CHART Management Consultants
FL, USA
Joseph J. Biehl
Consulting Services
ProPharma Group, USA
Robert Beall
AD ProPharma Group , USA
Cynitha J
Lean Compliance Partners
FL, USA
Christopher Joseph Devine
President & CEO
Devine Guidance International Inc., USA
Ravi
General Manager
BioSPEQ Inc., USA
Tina
Gerson Lehrman Group, USA
Philip Onigman
Bio-technology Consultant
Boston, USA
Kaitlin Bratlie
Chemical & Biological Engineering
Iowa state University, USA
Michel N. Mifundu
Kyoto University, Japan
Elizabeth N De Gaspari
Prof Advisor of Biotechnology program
Sao Paulo University, Brazil
Igho Onakpoya
University of Oxford, UK
Fernando Geijo Caballero
Development Team Consulting
Barcelona, Spain
vijaya shinde
Director of Sai Pharmaceutical consultant
, India
Rajinsh Gupta
Research Officer
Center for Advance research and Development, India
Prashant G
Piramal Healthcare Limited
Mumbai, India
Divya kanwar Bhati,
Indian Institute Of Health Management Research, , India
Tianchang Zuo
NNE Pharmaplan, Tianjin, China
Eyob
lecturer of Pharmacology
Debre Birhan University
, Ethiopia
Track 1: Quality Control Audit's in Clinical Laboratories
Track 1-1
Clinical research and phases of research
Track 1-2
Digitizing in quality control, inspection & reverse engineering
Track 1-3
Pharmacovigilance
Track 1-4
Pharmacokinetics and Pharmacoepidemiology
Track 2: Drug Design and Drug Manufacturer Precautions
Track 2-1
Drug safety communication
Track 2-2
Formulations & validation of drugs
Track 2-3
Medicinal chemistry in drug development
Track 2-4
Drug safety strategies to the risk compounds
Track 2-5
Lyophilization process development for proteins
Track 3: GLP & GMP
Track 3-1
OECD guidelines for testing of chemicals
Track 3-2
FDA / EU guidelines
Track 3-3
Verification and Validation
Track 3-4
Current Good Manufacturing Practice (cGMP)
Track 4: Clinical Data Management
Track 4-1
Validation of rules and regulations
Track 4-2
Patent rights of drugs
Track 4-3
Risk assessment of drugs
Track 4-4
Stability indicating method validation
Track 5: Analytical Method Development and Validation for Therapeutic Proteins
Track 5-1
Validation of HPLC methods in pharmaceutical analysis
Track 5-2
Analytical technologies for biopharmaceutical development
Track 5-3
Application of QbD and DOE in method development and validation
Track 5-4
Manufacturing process for therapeutic proteins
Track 5-5
Six sigma applications in method validation
Track 6: International Perspectives on Quality Assurance and New Techniques
Track 6-1
Successful method transfer strategies
Track 6-2
Socioeconomic impact on advanced technologies
Track 6-3
NMR spectroscopy and hyphenated technology
Track 6-4
Quality control in radiochemical analysis
Track 6-5
Next generation sequencing technology
Track 7: Novel Methods of Purification by Downstream Processing
Track 7-1
Designing & development in medical devices
Track 7-2
Bio- Analytical methods
Track 7-3
Methods of recovery and purification
Track 7-4
Vaccine and antibody production
Track 8: Food and Nutraceuticals
Track 8-1
Quality control in a typical food processing system
Track 8-2
Food inspectorate, analytical services, and compliance unit
Track 8-3
Hazard analysis and critical control points (HACCP)
Track 8-4
Food law and accompanying regulations
Track 9: Technology Transfer for Industrial pharmaceuticals
Track 9-1
Recombinant protein & complex biologic development & production
Track 9-2
Pharmaceutical quality management software systems
Track 9-3
Master control validation services
Track 9-4
Interfacing analytics with process development and formulations
Track 10: Quality Management and Quality Improvement in Research
Track 10-1
Identifying and controlling critical quality attributes
Track 10-2
Quality assessment and validation of computerized systems in clinical trials
Track 10-3
QA and compliance-audits and inspections
Track 10-4
Quality improvement in human research protection programs