Description of event:
International Conference on QA, QC and Validation
International Conference on QA, QC and
Validation at DoubleTree by Hilton Philadelphia Center City, USA.
Quality control-2012 is a remarkable event which brings together a unique and International mix of large and
medium Health & Research and
diagnostics companies, leading universities and research institutions making the conference a perfect platform to share experience, foster collaborations across industry and academia and evaluate emerging technologies in improving the quality of product across the globe.
Quality control is an approach that extends beyond ordinary statistical
quality control techniques and quality improvement methods. It implies a complete overview and re-evaluation of the specification of a product, rather than just considering a more limited set of changeable features within an existing product.
Quality control-2012 will schedule and coordinate all meetings with our Editorial Board Members and other experts in quality in Research & Production field across the World. The scientific program paves a way to gather visionaries through the research talks and presentations and put forward many thought provoking strategies on QA, QC and
Validation.
Conference highlights the following topics:
•
Quality Control Audit’s in
Clinical Laboratories
•
Drug Design and
Drug Manufacturer Precautions
•
GLP &
GMP
•
Clinical Data Management
•
Analytical Method Development and
Validation for
Therapeutic Proteins
• International perspectives on Quality Assurance and New Techniques
• Novel Methods of
Purification by Downstream Processing
• Food and Nutraceuticals
• Technology Transfer for Industrial pharmaceuticals
• Quality
Management and Quality Improvement in Research
Omics Group 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.
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
Venue:
DoubleTree by Hilton Philadelphia Center City
237 S Broad St, Philadelphia, United States
Contact us:
Conference Secretariat: QA, QC and
Validation OMICS Group Conferences
5716 Corsa Ave., Suite 110,
Westlake, Los Angeles,
CA 91362-7354, USA