Louis Garguilo
ARTICLES BY LOUIS
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2/26/2020
In the course of an hour, Frank Gupton mentions the highest level government officials; Janet Woodcock of CDER; Scott May of Eli Lilly; an ongoing project with DARPA; and others. They all come to the professor for help with U.S.-based manufacturing, and particularly the art of continuous manufacturing.
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2/19/2020
In 2005, Stephen Langille was the FDA liaison to the USP Parenteral Products - Industrial Expert Committee. He and others were concerned with the number of injectable drug product batches rejected or recalled because of “visible particulate matter.” The situation grew worse over the years. But now Langille offers advice on how you — and your CDMOs — can prevent issues from occuring.
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2/18/2020
What happens – or continues not to happen – next with the coronavirus is critical to the future of global pharmaceutical development and manufacturing industry’s supply chains. But what lessons will we draw from the crisis?
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2/5/2020
I suppose it was inevitable. After years of escalating one-upmanship in the CDMO industry, it was only a matter of time before we got the “biggest CDMO on the planet” announcement. But more details were needed. We’ve now got them for you.
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2/3/2020
We may think we’ve been through this before with other coronaviruses such as SARS and MERS … but this time it feels different, like a larger confluence of too many overlapping and unstable tectonic plates.
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2/3/2020
Still today one of the least explored dimensions of drug development and manufacturing outsourcing is the “no-choice partnership.” This might be an inherited relationship, or when unique platforms, technologies, and therapies leave few CDMOs that can actually assist. We did more exploring for you.
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1/29/2020
Among the digital technologies that biopharma organizations can target for investment, the first choice is cyber security. But is enough of that investment steered to supply chains? And what of cyber security at CDMOs? Here’s a detailed analysis.
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1/23/2020
Michael Mulkerrin, VP, Head of CMC, ADC Therapeutics, has been a part of the biopharma industry for 35 years, the first 16 at Genentech. He’s a member of the Council of Experts, United States Pharmacopeia (USP). Recently, he offered some sage advice regarding CDMO relationships.
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1/15/2020
What equipment is essential at the CDMO assisting with your cell and gene therapy development and production? I’ve received some details via an investigation into Harvard’s Center for Advanced Biological Innovation and Manufacturing, and a discussion with the CEO & President of GE Healthcare Life Sciences.
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1/13/2020
Bottlenecks and backlogs in development and production of cell and gene therapies. Harvard to the rescue. Actually, Harvard with partners, such as companies familiar to Outsourced Pharma readers. But what will go into the the $50 million Center for Advanced Biological Innovation and Manufacturing? We’ve got exclusive details.