STAT
JULY 7, 2023
WASHINGTON — A House subcommittee will next week mark up a package of public health bills, including pandemic-preparedness legislation, according to five lobbyists. The House Energy & Commerce Committee hasn’t yet announced the markup, and the lobbyists didn’t know the exact date.
European Pharmaceutical Review
AUGUST 23, 2022
On- or in-dose authentication means that a security measure or anticounterfeit feature is integrated with the dosage form itself, offering product verification and traceability embedded into each medicine, rather than on the secondary package” WHO estimates that >50 percent of the drugs for sale on the internet are fake. References.
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European Pharmaceutical Review
JUNE 24, 2022
It is too early to say because we have not seen the whole package of measures yet. THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION; 2006. THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION; 2006. The cost of opportunity – A study on pharmaceutical R&D costs [Internet].
European Pharmaceutical Review
FEBRUARY 7, 2023
Launch of the EU pharmaceutical package The European Commission plans to commence initiatives relating to the European Pharmaceutical Strategy (strategy) with the publication of the revised EU pharmaceutical package scheduled during the first quarter of 2023.
European Pharmaceutical Review
NOVEMBER 4, 2022
6 In March 2021, following a pre-NDA meeting, the company issued a release stating “[the company] has concluded that the clinical data package for Tesetaxel is unlikely to support FDA approval”, and the programme was subsequently terminated. 2006 [cited 7 September 2022];17(5):735-749. References. Hennenfent K, Govindan R.
BuzzRx
JANUARY 29, 2023
Keeping Sudafed products behind the counter, along with other regulations, was mandated by the FDA in 2006 because pseudoephedrine, the main ingredient in Sudafed products, can be used illegally to make methamphetamine. Read the package label carefully to check the right product and dosage for your child. Is Sudafed OK to take daily?
Pharmaceutical Technology
NOVEMBER 24, 2022
Study designs can be conventional, hybrid, or tracer studies, which can all generate the required data and be suitable to form part of the eventual regulatory submission data package. Since 2006, Quotient Sciences has provided radiolabeled clinical research for the pharmaceutical industry at our Nottingham, UK, site.
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