Eli Lilly

Activities: Manufacturing Cardiovascular Pharmaceutical

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  1. The three musketeers of pharmaceutical quality control GMP, GAMP5, and 21CFR11 explained
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    What is ISO 8 cleanroom classification? Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
  3. Germfree mobile cleanroom finishes pilot programme for hospital lidocaine production Modular cleanroom expert Germfree and pharma expert ODP are now working to expand a pilot programme after a successful six months of producing medications at North Mississippi...
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    Integrity testing of HEPA filters: A practical approach Filtering the air in aseptic process areas is critical to maintaining the cleanliness of the production environment. Jesus Casas provides tips to ensure HEPA filters are fit...
  5. Mary Marcus appointed CEO of NewAge Industries, Inc.

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Eli Lilly plans $400m investment in manufacturing technologies

Investments to enhance existing manufacturing facilities that make insulin, add capacity for diabetes medicines and prepare for future medicines
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ISPE names Facility of the Year 2019

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Eli Lilly's modernisation plan cuts 250 jobs in France

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Energy management

<p>For years, cleanroom operators have put product safety and yields top of the agenda, giving energy efficiency a lower priority. The BSI’s 2010 Cleanroom Conference unveiled new standards that demand a greener ethos. Susan Birks reports
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