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OMICS Group�s 2nd World Congress on Pharmaceutics & Novel Drug Delivery Systems

Theme: To showcase the cutting edge technologies in Pharmaceutics & Strategies of Drug Delivery.

Dates : 20-22 February 2012
Venue: San Francisco Airport Marriott, USA

Tel: Fax: Toll Free:
+1-650-268-9744 +1-650-618-1414 +1-800-216-6499

Website:
http://www.omicsonline.org/pharmaceutica2012/
Submit Your Abstract Online at: http://omicsonline.org/pharmaceutica2012/abstract.php
(or)
E-mail to: pharmaceutica2012@omicsonline.org

We warmly invite you to attend and submit your abstract to 2nd World Congress on Pharmaceutics & Novel Drug Delivery Systems
 
Pharmaceutica-2012 is comprised of 10 tracks and 43 sessions designed to offer comprehensive sessions that address current issues in Pharmaceutics & Drug Delivery Research. You can register the whole conference or select a single track or register for special service package that you want for your participation. Abstracts for the following proposed or related topics are accepted.
 
Please submit your abstract to any of the following tracks.
Track 1: New Technology of Drug Delivery Systems
Track 1-1: Sustained, Controlled or Modified-release Drug Delivery
Track 1-2: Prodrugs for Better Efficacy
Track 1-3: Electronically Controlled Drug Delivery Sysytems
Track 1-4: Biocompatible Polymers and Biopolymers
Track 1-5: Formulation and Drug Delivery Development of Poorly Soluble Drugs
Track 1-6: Gene and Cell Therapy
Track 2: Development of Personalized Medicine
Track 3: Biopharmaceuticals Development
Track 3-1: Biopharmaceutics and Formulation Development
Track 3-2: Role of PK/PD in Product Development
Track 3-3: Drug Development of Pediatrics: Formulation and Regulatory Aspects
Track 3-4: Bioavailability and Bioequivalence in Disease State
Track 4: Identification and Characterization of Drugs
Track 4-1: Characterization of Synthetic and Natural Products
Track 4-2: Structural Analysis: Characterization of Process or Product Related Impurities and Degradants
Track 4-3: Instrumental Methods for Identification and Characterization
Track 4-4: Metabolite Characterization: Drug Discovery
Track 4-5: Advanced Techniques in Structure Characterization
Track 5: Quality Management System in Pharmaceutical Industry
Track 5-1: Pharmaceutical Development & Quality Systems
Track 5-2: Quality Assurance and Quality Control for Pharmaceutical Development
Track 5-3: Quality Assessment for Pharmaceutical Products
Track 5-4: Food and Drug Safety
Track 5-5: Quality by Design: Broadening the Application and Sharing the Learnings
Track 6: Pharmacokinetic Considerations of Drug Delivery
Track 6-1: Pharmacokinetic Parameters for Drug Disposotion
Track 6-2: Pharmacokinetic Parameters for Drug Input
Track 6-3: Pharmacokinetic model for presystemic metabolism
Track 6-4: BA/BE studies of Pharmacokinetic Drug Interactions
Track 7: Trends in Drug Delivery Systems of Global Market
Track 7-1: Global Needs and Strategies for Novel Dosage Forms
Track 7-2: Generic Development of Drug Delivery Systems
Track 7-3: Product Planning, Technology Evaluation and Product/Brand Management
Track 7-4: Successful Drug Discovery from the Research Lab to the Marketplace
Track 8: Novel Drug Delivery System Technology Targeting Different Route of Administration
Track 8-1: Oral, Transmuco Adhesive and Buccal Drug Delivery
Track 8-2: Rectal and Vaginal Drug Delivery
Track 8-3: Nasal and Inhalable Drug Delivery
Track 8-4: Transdermal and Topical Drug Delivery
Track 8-5: Ocular Drug Delivery
Track 8-6: Novel Approaches in Drug Delivery
Track 9: Nanotech for Drug Delivery
Track 9-1: Biocompatible and Biodegradable Materials for Drug Nanoparticles
Track 9-2: Controlled Delivery of Nanoparticles in DDS
Track 9-3: Nanoparticles as Drug Carrier in DDS
Track 9-4: Site-Directed Controlled Nano-drug Delivery Systems
Track 10: Regulatory Issues, Quality Control, and Business Development
Track 10-1: Clinical Trials in Emerging Markets
Track 10-2: Benefit/Risk Assessment during Drug Development
Track 10-3: Safety and Quality Regulation
Track 10-4: Pharmacovigilance and Safety management
Track 10-5: Regulatory challenges in Nano and Biotech Therapeutics