7^th Annual Global Pharma Summit August 22-24, 2016 New Orleans, Louisiana, USA

Pharmaceutical Preformulation

Preformulation studies track of the Global Pharma Summit involves the focus on characterization of a drug's physical, chemical, and mechanical properties in order to choose what other ingredients (excipients)  should be used in the preparation.Global pharma companies are mainly focussing on the the studies viz., drug stability, drug-excipient compatibility enleash scale up problems. Polymorphism is a specific characteristic that is to be considered prior to formulation, in order to select the type of tooling and other parameters this character of the drug and excipients play a crucial role.

The pharmaceutical market been increasingly more affected through laws and regulations but has shown continuous growth as the diagnosis and understanding of diseases and condition has evolved and improved. BCC Research report’s cover the latest pharmaceutical market and provide in-depth market analysis, forecasts, trends, patent analysis, and profiles of major players within the markets. Comprehensive analysis of clinical studies for biopharmaceuticals, prevention and treatment of certain cancers, coagulants and non-coagulants are all within the range of pharmaceutical markets covered in BCC Research reports. Drug devices, instrumentation and inhibitors are some of the many other areas covered.

The analytical aspects of the drug and excipients used in the formulation should be highlighted with the type of interactions that might be possible in which analytical methods and evaluation are useful. Polymorphism is a specific characteristic that is to be considered prior to formulation, in order to select the type of tooling and other parameters this character of the drug and excipients play a crucial role.

• Biopharmaceutics and Biotherapeutics
• Drug designing
• Drug Selection
• Drug-excipient compatibility
• PK-PD Modeling of Drugs
• Accelerated Stability Studies
• Solubility Hindrance
• Multiple dosing
• Drug-dose safety
• Analytical Method Evaluation
• Scale-Up problems
• CDRH Transparency

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