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Potential Governing Body Emerges For DSCSA Tracing Of US-Marketed Drug Packages

 
• By Joanne S. Eglovitch

The idea of establishing a non-profit governance group to coordinate the package-level tracing of pharmaceuticals through the US distribution chain that DSCSA requires drew widespread support at a May 1 PDSA meeting in Washington, DC. PDSA wants to get the group up and running by October.

Politicians or corporate officers group authority people talks sitting at round table. Big war room. Negotiations conversation conference hall, boardroom or meeting room. Flat vector illustration - Vector

A vision is emerging and gaining buy-in across industry sectors that would establish an industry led governance board to help set up an electronic interoperable verification and tracing system for policing counterfeit drugs marketed in the US, due in November 2023 by law.

The plan is for private sector firms that participate in the biopharmaceutical supply chain such as manufactures, wholesalers and distributors to create a non-profit governance group for the interoperable system for tracing pharmaceutical

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More from Manufacturing

US FDA’s Expanded Surprise Foreign Inspections: Impact And Enforcement Hoops

 
• By Anju Ghangurde

As the US FDA expands unannounced foreign inspections building on pilots in India and China, experts expect higher scrutiny of overseas sites and perhaps even an industry shakeout in the longer term, though staffing and enforcement challenges could slow things down.

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• By Jessica Merrill

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• By Sue Sutter

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Pharma Predicts Modest Tariff Impact, Depending On What Comes Next

 
• By Jessica Merrill

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More from Compliance

Switzerland Simplifies Imports Of Unauthorized Drugs To Tackle Drug Shortages

 
• By Eliza Slawther

Swiss authorities have introduced temporary measures that will make it easier for health care professionals to import medicines that are either not authorized or not available in Switzerland, which will particularly benefit pediatric drugs, in light of ongoing shortages.

Aragen’s CEO Says NIH Funding Cut Means Less R&D Money, And Tariffs Would Add To Woes

 
• By Vibha Ravi

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US FDA Retirements Continue Unabated With Drug Inspectorate Leaders, Former Chief Counsel

 
• By Sue Sutter and Derrick Gingery

Alonza Cruse, director of the Office of Human and Animal Drugs Inspectorate, and two other senior inspection officials are departing, along with Mark Raza, chief counsel from 2021 until January.