Call for Abstract
Scientific Program
International Conference and Expo on Parenterals & Injectables, will be organized around the theme “Exploring the Challenges in Parenterals and Injectables: Manufacturing and Sustainability”
Parenterals 2015 is comprised of 14 tracks and 79 sessions designed to offer comprehensive sessions that address current issues in Parenterals 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 1-1Generic sterile injectable drug-advances and drawbacks
- Track 1-2Route of administration
- Track 1-3Injections: a dangerous engine of disease
- Track 1-4Reported factors leading to injection overuse
- Track 1-5Misconceptions about injections among prescribers
- Track 1-6Factors influencing absorption and bioavailability of medications etc..
- Track 2-1In Situ Forming Parenteral Drug Delivery Systems
- Track 2-2lipid nanoparticles for injectable delivery
- Track 2-3Parenteral lipid nano dispersions
- Track 2-4Injectable liposomes etc..
- Track 3-1Formulation and Drug Delivery Strategies
- Track 3-2Advances & Progress in Drug Design
- Track 3-3Rational Drug Design
- Track 3-4In-silico Drug Design and in-silico screening
- Track 3-5Drug delivery case studies
- Track 3-6Clinical Pharmacology in Drug Development
- Track 3-7Development of sustained-release drug delivery systems etc..
- Track 4-1Drug Discovery in Preclinical Research
- Track 4-2Pharmacology in Drug Discovery
- Track 4-3Innovative Drug Discovery and Nanotechnology
- Track 4-4De-risking Drug discovery
- Track 4-5In silico approaches to fragment-based drug design
- Track 4-6Novel approaches in drug discovery
- Track 5-1Market opportunities
- Track 5-2Market dynamics
- Track 5-3Meeting standards set by regulatory authorities
- Track 5-4Threat of substitutes
- Track 5-5Wider applications in parenterals etc..
- Track 6-1Impact of silicone oil on delivery
- Track 6-2Overcoming variability in glass syringes
- Track 6-3Vapor phase polymers and its challenges etc..
- Track 7-1New developments in delivery devices
- Track 7-2Improvements in micro liter dosing
- Track 7-3Aseptic transfer mechanisms
- Track 7-4Glass and plastic syringes-recent advances
- Track 7-5Injection site leakage-effect on drug dose etc..
- Track 8-1Enhanced sterilization methods for pre-filled syringes
- Track 8-2Innovations with of pre-filled syringes systems
- Track 8-3Materials in the preparation of prefilled syringes
- Track 8-4Plastic or polymers used in pre-filled syringes
- Track 8-5Sterilization and validation protocol for pre-filled syringes
- Track 8-6Pre-filled syringes in market place
- Track 8-7Customization of pre-filled syringes to overcome its drawbacks and etc..
- Track 9-1Clinical Guidelines for Parenteral Nutrition Compounding, Labeling, and Dispensing
- Track 9-2Parenteral Nutrition Safety Consensus Recommendations
- Track 9-3Safe Practices for Parenteral Nutrition Formulations
- Track 9-4Intravenous Admixture System
- Track 9-5Stability of parenteral admixtures
- Track 9-6Incompatibilities in parenteral admixtures etc..
- Track 10-1Vaccines for parenteral use
- Track 10-2New parenteral vaccine approaches
- Track 10-3Parenteral vaccines Against Infectious Diseases and Cancers
- Track 10-4Parenteral norovirus vaccine formulations
- Track 10-5live parenteral vaccines
- Track 10-6Intravenous vaccines
- Track 10-7Risk assessment and management of parenteral vaccine usage etc..
- Track 11-1Time to peak serum concentration by different modes of administration
- Track 11-2Sequential and prolonged parenteral antibiotics
- Track 11-3Pharmacokinetic advantages of parenteral over oral administration
- Track 11-4Therapeutic index and toxicity of Parenterals
- Track 11-5Clinical trials in parenterals and injectables etc..
- Track 12-1Infusions with syringe pumps
- Track 12-2Factors influencing the safety of device
- Track 12-3Modification of device features for enhanced patient comfort
- Track 12-4Quality Concerns and Considerations Injectable Products
- Track 12-5Analysis and safety evaluations of injectables and leachables and etc..
- Track 13-1Developing and registering commercially successful injectable drug products
- Track 13-2Basic elements and requirements behind the regulation of Drug delivery combination products
- Track 13-3Risk Management for Temperature Controlled Distribution
- Track 13-4Regulatory issues about the standardization of pre-filled syringes
- Track 13-5Injectable and medical devices.
- Track 13-6Human factors and usability
- Track 13-7Clinical or Marketing Approval applications of parenteral
- Track 14-1Wearable pre-filled syringes
- Track 14-2Drug injections into the eye
- Track 14-3New sterile packaging connection systems
- Track 14-4Novel needle technologies
- Track 14-5Advanced innovation for a new generation of needle free plastic pre-filled syringes
- Track 14-6Modern blow-fill-seal processing etc..