Tag Archives: Eli Lilly

Root Cause Analysis For USP Dissolution and Tablet Disintegration Studies

USP dissolution testing is a standard method in pharmaceutical industry to characterize dissolution performance of solid dosage forms. Continue reading

Process Development at AIChE 2010

While reviewing the agenda for next month’s American Institute of Chemical Engineers (AIChE) Annual Meeting, I noticed a number of papers and posters discussing process development in pharmaceuticals, chemicals, and academia: Continue reading

Symposium on Green Processing in the Pharmaceutical & Fine Chemical Industries

Last week, John Tedesco and I had the privilege to attend the 3rd International Symposium on Green Processing in the Pharmaceutical & Fine Chemical Industries in Boston, MA. Continue reading

Congratulations to 17th IPDC Award Winners: Best Paper Award presented to Dr. Martin Johnson of Eli Lilly

METTLER-TOLEDO-International-Process-Development-Conference

Martin Johnson, Eli Lilly

METTLER TOLEDO is pleased to announce that Dr. Martin D. Johnson of Eli Lilly won the award for Best Paper at the 17th International Process Development Conference (IPDC).

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