Call for Abstract
Scientific Program
4th International Summit on GMP, GCP & Quality Control, will be organized around the theme “New Paradigm Approach for Manufacturing Excellence and Quality Standards”
GMP Summit 2015 is comprised of 13 tracks and 80 sessions designed to offer comprehensive sessions that address current issues in GMP Summit 2015.
Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.
Register now for the conference by choosing an appropriate package suitable to you.
- Track 1-1Traditional role of contract manufacturing
- Track 1-2Quality over quantity in contract manufacturing
- Track 1-3Microbiological basics, Sterilization processes & Environmental monitoring
- Track 1-4Requirements for successful contract manufacturing partnerships
- Track 1-5Six sigma approaches and lean manufacturing
- Track 2-1GMP for active pharmaceutical products
- Track 2-2GMP for biotechnological products
- Track 2-3Licensing in pharmaceutical production
- Track 2-4GMP for biopharmaceuticals
- Track 2-5cGMP Quality Principles for Biologics and Medical Devices
- Track 3-1Roles of pharmaceutical inspection convention and co-operation scheme (PIC/S)
- Track 3-2FDA regulations and CFR
- Track 3-3EU-GMP guidelines
- Track 3-4WHO-GMP guidelines
- Track 3-5International Regulatory Affairs
- Track 3-6Importance of audit in pharmaceutical industry
- Track 4-1Pre-formulation development
- Track 4-2Formulation development
- Track 4-3Optimization of existing formulations
- Track 4-4Product/Process optimization
- Track 4-5Novel formulations for improved delivery of existing dosage forms
- Track 4-6Physico-chemical testing
- Track 4-7Process scale-up
- Track 4-8Technology transfers
- Track 4-9Batch manufacture
- Track 5-1Hazard analysis and critical control points (HACCP)
- Track 5-2Quality control in a typical food processing system
- Track 5-3Cleaning, disinfection and hygiene
- Track 5-4Validation Practices in the Food Industry
- Track 5-5Current food industry good manufacturing practices
- Track 5-6Food, Drug and Cosmetic Act (FDCA)
- Track 6-1Sterility assurance and sterility testing
- Track 6-2Microbial assays
- Track 6-3Validation of microbial recovery
- Track 6-4FDA 510k Testing
- Track 6-5Contamination control, cleaning, disinfection and hygiene
- Track 6-6QC in Microbiology lab
- Track 7-1Role of ICH in designing GCP principles
- Track 7-2Principles of GLP in vitro Studies
- Track 7-3OECD guidelines for the testing of chemicals
- Track 7-4Good Laboratory Practices (GLP) for Pre-Clinical Testing
- Track 7-5IEC-GCP regulations
- Track 7-6Pre-clinical trails
- Track 7-7Clinical trails
- Track 7-8SAS Programming, Usage in Pharmaceutical Industry
- Track 8-1Facts About Current Good Manufacturing Practices (cGMPs)
- Track 8-2Good Automated Manufacturing Practice (GAMP)
- Track 8-3Current Trends in the FDA
- Track 8-4GMP/GCP Interface & GMP audits
- Track 8-5GMPs for OTC and Cosmetic Products – Global Requirements
- Track 9-1Effective Internal and External Quality Assurance Auditing
- Track 9-2Quality Risk Management
- Track 9-3Quality inspection and Auditing
- Track 9-4Quality by Design(QbD)
- Track 9-5Quality Metrics & Total quality management
- Track 10-1The role of Quality Impact Assessment & effectiveness checks
- Track 10-2Quality control in Microbiology
- Track 10-3Quality control in Food Industry
- Track 10-4Quality control in Textile Industry
- Track 10-5Drug product stability testing
- Track 10-6Analytical quality control
- Track 10-7Corrective and preventative action (CAPA)
- Track 10-8Quality control in project management
- Track 10-9Quality Control softwares and tools
- Track 10-10Analytical method development
- Track 11-1Good Distribution Practices
- Track 11-2Manufacturing Execution System (MES)
- Track 11-3New GDP guidelines
- Track 11-4Cold chain storage
- Track 11-5Supply chain integrity
- Track 12-1Design, monitoring, and control of manufacturing processes and facilities
- Track 12-2Maintenance, calibration and validation of equipment
- Track 12-3Role of qualified person and quality Indicators in GMP
- Track 12-4Reliability and reproducibility of processes
- Track 12-5Quality management systems
- Track 13-1Cleaning validation and process validation of biopharmaceuticals
- Track 13-2Analytical method validation and computer system validation
- Track 13-3Change Control
- Track 13-4Phases of Validation
- Track 13-5HVAC system validation