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Steriline to exhibit its Robotic Vial Filling Machine at ACHEMA 2024

Express Pharma

Steriline, the European manufacturer of standard and robotic lines for the aseptic processing of injectable drugs, will exhibit at Achema 2024, from June 10 to 14.It It will showcase the new technologies developed to upgrade its zero-loss philosophy, to better meet the sustainability needs of the pharmaceutical industry.

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IPA questions FAERS data interpretation in the Ohio State University study

Express Pharma

IPA also addressed concerns regarding transparency in drug manufacturing locations. It noted that US law requires complete manufacturing addresses to be printed on generic drug packaging and listed in the FDAs Orange Book database.

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Bayer’s Eylea market grip set to slip as Alvotech biosimilar closes in

Pharmaceutical Technology

Indeed the $9.5bn in sales it generated in 2024, which includes revenue from a high-dose version, means it is one of the top-selling drugs in the world. Eylea’s glory days ending Alvotech is just the latest pharma company to spur an Eylea biosimilar into the European market after Bayer’s blockbuster lost regulatory exclusivity in mid-2024.

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Line clearance procedure and reconciliation in GMP

GMPSOP

Proper line segregation involves physically separating different lots of starting materials, labeling components, and printing matters, many of which look similar. Before filling and labeling, you should thoroughly examine the filling line using a standard operating procedure. Please look at the labeling operation in the picture below.

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The Pandemic Treaty and the opportunity to end ‘vaccine apartheid’

pharmaphorum

The negotiations over the treaty are being hosted through the World Health Organization (WHO), with plans to officially adopt a binding agreement sealed by the United Nations health agency’s member countries in May 2024. The UN Special Rapporteur on contemporary forms of racism, E.

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NHC Submits Comments on FDA Draft Guidance on AI to Support Regulatory Decision-Making for Drugs/Biologics

Putting Patients First Blog

Furthermore, FDA guidance should include requirements for clear labeling and disclosure of any remaining performance limitations or biases, ensuring clinicians and patients are aware of potential constraints in real-world contexts. 3 ,4 The NHC is uniquely positioned to provide input on this issue.

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PHARMAP 2024 held in Amsterdam, marks its fourth edition

Express Pharma

The event brought together over 330 professionals from across the industry’s value chain Pharmaceutical Manufacturing and Packaging Congress (PHARMAP 2024) was held in Amsterdam, Netherlands on April 22-23, 2024. Among the attendees, contract manufacturing organisations, service providers and experts were present.

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