Pharmaceutical Technology Europe
One of the most important skills any editor must possess is the ability to listen to their audience — without feedback, we don't get an opportunity to develop our publications; to not act on feedback shows plain ignorance. I must, therefore, give my personal thanks to the many hundreds of readers who participated in the Pharmaceutical Technology Europe (PTE) editorial and readership survey, which we conducted earlier this summer. Your comments and opinions will help us develop PTE, and we already have a number of exciting plans for 2006. Stay tuned!
One of the most important skills any editor must possess is the ability to listen to their audience — without feedback, we don't get an opportunity to develop our publications; to not act on feedback shows plain ignorance. I must, therefore, give my personal thanks to the many hundreds of readers who participated in the Pharmaceutical Technology Europe (PTE) editorial and readership survey, which we conducted earlier this summer. Your comments and opinions will help us develop PTE, and we already have a number of exciting plans for 2006. Stay tuned!
Gurminder Marwaha
Staying with this year, however, you will have noticed PTE's new editorial advisory board (EAB) members. An EAB is crucial to any magazine or journal wanting to publish factually accurate features that help shape and develop the industry in which it serves — and this magazine is no different. I now have the opportunity to thank those who served on the previous EAB for their input; I would also like to publicly welcome my new EAB members, who are all internationally recognized experts.
Onto more immediate matters and life doesn't look rosy for Merck after a US jury found the drugs' manufacturer, negligent when a patient (Robert Ernst) died suddenly whilst on Vioxx. This case has serious repercussions because it is now likely to open the floodgates for other users to sue. Perhaps we are going to start seeing a trend whereby the patient power that exists in the US will manifest itself to Europe. According to reports (bbc.co.uk) it has been estimated that Vioxx could have caused almost 28000 heart attacks or deaths since it was approved for use in 1999, and more than 4200 lawsuits have been filed against the firm over the drug. Some analysts have calculated that the Vioxx episode may represent a liability of as much as $18 billion. The company has reportedly set aside $675?million to fight Vioxx suits.
After the ruling, Merck's attorney, Jonathan Skidmore, said: "There is no reliable scientific evidence that shows Vioxx causes cardiac arrhythmia, which an autopsy showed was the cause of Mr Ernst's death." He also added that the Texas case was a "shot across the bows" for Merck. I would say it is a shot across the bows for all drug manufacturers — they have been warned.
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines
April 30th 2024In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
FDA Approves Novartis Oral Treatment for Adults with C3 Glomerulopathy
March 25th 2025Fabhalta (iptacopan) received a positive opinion for treatment of C3G from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) and has been approved twice before by FDA.
Drug Solutions Podcast: Gliding Through the Ins and Outs of the Pharma Supply Chain
November 14th 2023In this episode of the Drug Solutions podcast, Jill Murphy, former editor, speaks with Bourji Mourad, partnership director at ThermoSafe, about the supply chain in the pharmaceutical industry, specifically related to packaging, pharma air freight, and the pressure on suppliers with post-COVID-19 changes on delivery.