Remove 2017 Remove Packaging Remove Vaccines
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STAT+: Pharmalittle: Italy probes Pfizer over profit transfers; FDA postpones meeting for OTC birth control pill

STAT

This calls for celebration with a cup of stimulation, and we are opening a new package of Pumpkin Spice for the occasion. The investigation began in February and covers 2017, 2018, and 2019. Autumn, after all, is in full swing. Meanwhile, our ever-growing to-do list requires attention. Sound familiar?

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Prednisone for gout: Dosage, safety, and more

The Checkup by Singlecare

Prednisolone ( Prednisolone is the active form, whereas prednisone has to be converted to prednisolone by the liver before it can work) , a powerful anti-inflammatory medication, has been shown effective as a first-line treatment for gout in studies such as those from 2016 and 2017. It might work quickly, too.

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How automation can help to address supply chain challenges in pharma

pharmaphorum

It’s imperative that all suppliers and distributors know if disruption is likely to occur, whether that be concerning incoming raw materials or outgoing packaged drugs. Better communication with traceable data. Mix ups in hand-offs are another large disruptor, especially when drugs have specific shipping requirements.

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Pre-Filled Syringes East Coast 2022

pharmaphorum

The past year has seen significant developments in the injectables landscape with the rapid introduction and development of vaccines in response to the pandemic, updates in regulations including the EU MDR and FDA guidance on bridging studies, and increasing industry acceptance of connectivity to aid the user experience. Secondary packagers.

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Streamlining Postapproval Submissions Using ICH Q12 & SCDM

ISPE

For changes requiring approval before implementation, once the necessary information has been submitted across regions, each health authority must review the data package and documentation based on local requirements. BioProcess International 15 (September 2017):24–47. Published July 2017. Macheras, and K. Tschorn, U.

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Message from the Chair an Exciting Year

ISPE

Tim Howard, who was Chair of the International Board from 2017–2018, helped by moderating the sessions. In addition, we took the Board on tours of Vetter’s facilities for sterile products and through all the production steps: compounding to fill-finish to automated visual inspection and secondary packaging. Thank you, Tim!

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FDA committee recommends AstraZeneca and Sanofi’s RSV prophylactic nirsevimab

Pharmaceutical Technology

After a long period without any new approvals, in May, the FDA approved GSK’s vaccine Arexvy for the prevention of LRTD caused by RSV in individuals 60 and older. On 31 May, the FDA also approved Pfizer’s vaccine Abrysvo in the same patient population.

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