Pharma Manufacturing 2013

Time:August 20-22, 2013

Country&Region: India

Venue:The Lalit Mumbai, India

Organizer:UBM India

A not- to- be missed event for Indian Pharma Manufacturers which not only concentrates on keeping them abreast of best practices and recent advances in Pharma Manufacturing but also aides in understanding implementation of these practices through practical examples, case studies, innovation hot-spots and workshops.

Pharma Manufacturing training series with focused sessions on challenging areas flagged by the top 33 pharma companies:

Failure Investigation: Learn from past failure investigation queries of regulators and techniques on how to avoid OOS-OOT
Process Validation: Clear your 3 batch confusion and be geared up for the upcoming regulatory compulsion on process validation
Operational Excellence: Save on cost, reduce process variability, lower DPM to achieve better OEETestimonials from

Pharma Manufacturing 2012

This was one of those conferences where I felt that the investment of time was worth .The topics were very focused and engaging and the view of regulator was an added value
Managing Director/CEO, Eisai

This conference will help me to initiate the concept of QbD, lean manufacturing and implement the new concept of Process Validation- Site
Head Quality, Fresenius Kabi Oncology Limited

This was very important to us with respect to new products introduction especially in regulated Markets. Changes in DMF filing and requirement of QbD as mandatory has given insight to development and document process starting from R&D
Vice President Operations, CALYX CHEMICALS & PHARMACEUTICALS LTD

Contact:UBM India

Tel: +91 (022) 61727001 / 022 61727272

Website:http://www.pharmamanufacturing-india.com/

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