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Adapting to the Disruption in the Pharma Industry: Leadership Challenges & Building Culture for Continuous Change View All Posts
Adapting to Disruptive Change in the Pharmaceutical Industry: The Pharmaceutical Industry continues to change at what feels like an exponential pace. What used to be a stable industry now faces almost continual re-shaping as the life cycle of R&D and commercialisation adapts to new players and shapers. New Pharma IQ columnist, Andrew Parsons explains. read more
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Raising the bar: 5 Areas for Improvement within the Pharmaceutical Outsourcing (CDMO model): Within the last few years the Pharmaceutical industry has taken a change in direction. Outsourcing (CDMO - external manufacturing model) has become a normal course of business. read more
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A Guide to Ensure FDA Audits & Inspections are Successful: How can FDA Audits & Inspections for FDF (Finished Dosage Form) manufacturers be successful? Know the process and requirements. read more
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Compounding Pharmacies or Manufacturers?: Columnist Tye Spillum reflects on the recent FDA initiative to identify & inspect several of the top compounding pharmacies manufacturing sterile products, which began earlier this year. read more
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CDMO Quality Agreements: Reviewing the purpose of the Quality Agreement and looking at what degree the customer will be integrated into the manufacturing process from a Quality perspective. Communication, roles, responsibilities, requirements, expectations, level of control, and the decision making process are a few of the key areas. read more
Events of Interest
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Compound Management & Integrity Online 2011
November 14, 2011
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Regenerative Medicine and Barriers to Commercialisation Online Summit 2011
October 25, 2011
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Electronic Laboratory Notebooks Online
December 2, 2011
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Drive Successful Commercial Product Launches through Effective Key Packaging
February 7, 2013
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