August 21 - 22, 2012
National and International experts discussing regulatory hurdles, engineering challenges and commercialisation strategies

Designing and creating an stable nano particle, sterilisation, scalability and regulatory clearances for commercialisation of nanomedicines are big challenge areas for generic and biopharma companies.

Key issues covered in the conference are:

•Overview of nanomedicines globally and what will be your ROI in future years
•Case studies on documentation, regulations and quality considerations when nanomedicines are exported
•Effective sterilisation techniques for nanocarriers
•Nanomedicine diagnostic and therapeutic advances
•Best stabilisation techniques for nanoparticles
•Innovative marketing and commercialisation strategies when promoting your products

Plus! – focused workshop dedicated to engineering challenges covering most relevant challenges including:

•Comparison of beads milling and high pressure homogenisation techniques
•Other techniques of formulation engineering
•Most efficient formulation techniques and measuring ROI

Key Highlights of this event are:

•Host of national and international experts discussing case studies of commercially launched products
•Representation from international regulatory bodies providing step-by-step guidance on your documentation and filing challenges
•Submit your case specific queries when registering and our expert speakers will surely provide clarifications
•Dedicated workshop to provide in-depth and practical solutions to your sterilisation and scalability challenges
•Network with senior-level decision makers with extensive expertise and multiple publications on nano technology

With an very focused and comprehensive agenda – Nanosuspensions 2012 will be aimed to provide most relevant, practical and implementable solutions for all you

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