PharmaAQ 2019

Pharmacetical Analysis & Quality Conference (PharmaAQ) 2019 is organized by Select Biosciences India Pvt. Ltd. and will be held from Dec 05 - 06, 2019 at Hyderabad, Telangana, India.

Overview
Quality Management systems of a Pharmaceutical company follow GMP guidelines and require that the analytical methods, followed for drug analysis, are robust and are developed following all validation principles. The second edition of the Pharmaceutical Analysis and Quality conference "Pharma AQ 2019" is a unique conference for analytical scientists working in the analysis of small and large molecules. This is a Pharmaceutical Industry focused event and is designed to discuss advanced analytical techniques like HPLC, Mass spectrometry etc., analytical method development, analytical techniques in biotechnology and many more. These techniques are followed as per WHO or ICH or FDA guidelines for assay development, thereby ensuring the quality of pharmaceutical products. 

This event will include discussions by Industry Experts from Pharmaceutical analysis and quality control fields, covering topics like analytical techniques, including HPLC, Mass, NMR, Raman, Hybrid instrumentation and software solutions to analytical problems, QbD approaches, validation parameters, analytical errors, meaningful data analysis etc. The organizers envisage bringing more and more overseas and industry scientists as speakers so that the delegates are able to derive maximum benefit from their expertise.

Agenda Topics
• Analytical Methods & Approaches
? Simultaneous Determination of Components by HPLC
? Analysis of Insoluble Components, Salt and Crystal-form Screening Studies
? Analysis of Solubility & Permeability Attributes for Solid Oral Drug Delivery
• Analytical Control Strategies
? Analytical QbD, PAT, QRM
• Chromatography and Separation Techniques
? Separation of Complex Mixtures and Biological Samples
• Advanced Analytical Techniques
? NMR, GC-MS/MS, LC-MC/MS, Raman
? ICP-MS, ICP-OES, 2DLC
? High-throughput FT Raman, X-ray Powder Diffraction, and Thermal Analysis
• Analysis of Peptides and Proteins
? Bioassays, Binding Assays, Enzyme Assays
? Physical & Chemical Methods
• Pharmaceutical Microbiology
? 21 CFR 211, Minimizing Contamination, Microbial Data Deviations
? Risk Assessment & Special Tests for Non-sterile Water-based Drug Products
? Pre-use, Post-sterilization Filter Integrity Testing (PUPSIT)
• GLP/GMP and Regulatory Audits
? cGMP Regulations, USP Methods
• Analytical Considerations for Stability Studies
? ICH Q3A(R2) & Q3B(R2), Impurity Profiling
? Extractable and Leachable
? OOS/OOT Results
• Meaningful Data Interpretation & Analytical Errors
? Reducing Analytical Variability

Fee:
Overseas Scientist $ 600
Overseas Business Delegate $ 800