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21 UChicago faculty receive named, distinguished service professorships

21 UChicago faculty receive named, distinguished service professorships
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Best practices to prevent the federal government from blowing its technology budget


Manufacturing & Service Operations Management Study Key Takeaways:
The study looked at archival data on 240 U.S. federal government technology programs across 24 federal agencies.
Researchers found that the practice of moving baseline targets is a key driver in continually increasing budgets for federal government technology programs.
The componentization of a program into smaller work units and increasing the level of competency in program management can dampen this increase, resulting in significant cost savings.
CATONSVILLE, MD, May 11, 2021 - With the U.S. federal government investing billions of taxpayer dollars in executing technology programs, wouldn t you like to know where this money is going? A new study has identified ways to reduce federal spending in the execution of these taxpayer-funded technology programs. ....

Anant Mishra , Kingshuk Sinha , Dwaipayan Roy , Us Federal Government Technology Programs , University Of Minnesota , Carlson School Of Management , Manufacturing Service Operations Management , Service Operations Management Study Key Takeaways , Service Operations Management , Baseline Changes , Government Technology Programs , Carlson School , Service Operations , ஒரு எறும்பு மிஸ்ரா , கிந்ஷூக் சீன்ஹா , பல்கலைக்கழகம் ஆஃப் மினசோட்டா , கார்ல்சன் பள்ளி ஆஃப் மேலாண்மை , உற்பத்தி சேவை செயல்பாடுகள் மேலாண்மை , சேவை செயல்பாடுகள் மேலாண்மை படிப்பு விசை எடுத்துச் செல்லுதல் , சேவை செயல்பாடுகள் மேலாண்மை , கார்ல்சன் பள்ளி , சேவை செயல்பாடுகள் ,

The case for creating excess capacity at the US Food and Drug Administration


Jeffrey Clemens, Parker Rogers
The public and political pressure on vaccine developers and global regulatory approval agencies has never been higher. The world has been eagerly awaiting any – and all – developments regarding vaccines and therapeutics required to fight the current Covid-19 pandemic. While the demand side is willing to pay almost any price for an effective and fast solution, unfortunately neither the drug development nor the drug approval process is designed to deliver speed and safety free of trade-offs. 
The dilemma faced by the regulators is simple. If regulators rush their review, they may end up approving a drug without adequately understanding its efficacy and safety, leaving room for unforeseen side-effects. These include safety issues around the drug itself, along with treatment dangers such as unsafe dosages and failing to highlight potentially dangerous drug interactions. Yet if regulators endeavour to understand all possible scenarios, it may ....

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