Swiss Medical Weekly Chooses Xpublisher for JATS XML-Based Publications
28.2.2023 17:09:00 EET | Business Wire | Press release
Xpublisher is the new publishing system for medical journal Swiss Medical Weekly (SMW). Working with Xpublisher enables SMW to publish JATS XML-based scientific articles online swiftly and reliably.
Swiss Medical Weekly uses Xpublisher
By choosing Xpublisher, the journal is pursuing a consistent XML and content-first approach to preparing media-independent content and automating its publication. The software’s integrated Xeditor assists the editorial team in formatting scientific articles based on the JATS XML article authoring schema. Xpublisher then facilitates a conversion of the XML data, customized for SMW, into an HTML format, which SMW uses for online publication through the CMS "Open Journal Systems" (OJS). “In parallel with migrating our website to Open Journal Systems, we were very interested in establishing an XML-first workflow based on the JATS format. We have analyzed several solutions and are absolutely convinced by Xpublisher and Xeditor. With the help of the Xpublisher GmbH team, we designed a customized system that clearly maps our processes and helps us to create all our articles in valid JATS XML. Since Xpublisher provided a JATS format, we not only imported the content, we also imported the metadata of every single previous article in our extensive archive into OJS completely automatically,” reports a pleased Dr. Natalie Marty, managing director of the SMW supporting association. The Xpublisher editorial system is available as SaaS in a highly secure cloud environment.
About Swiss Medical Weekly
Founded in 1871, the Swiss Medical Weekly is a medical journal with a long tradition. The SMW is a pioneer of the Diamond Open Access model. Even before the publication of the Berlin Declaration on Open Access, the journal had already introduced free open online access to all published articles, without charging authors publication fees. The articles are reviewed according to strict scientific criteria and published regularly online. The journal is published by the non-profit organization “Trägerverein Swiss Medical Weekly,” which aims to enable and advance publishing based on the Diamond model. For more information, visit www.smw.ch.
About Xpublisher GmbH
Xpublisher GmbH is a leading provider in the multichannel publishing space, delivering intuitive products for creating, managing, and automating magazine, book, and documentation publishing with Xeditor and Xpublisher. Xpublisher was founded in 2009 and is based in Munich, Germany. The company operates a US subsidiary and has been part of the Fabasoft Group since 2019. Numerous leading international companies and organizations in the publishing, aerospace, technology, education, and public administration sectors together with a host of other industries have already placed their trust in Xpublisher’s products.
For more information, visit www.xpublisher.com or follow us on LinkedIn and Twitter @Xpublisher.
To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.
View source version on businesswire.com: https://www.businesswire.com/news/home/20230228005220/en/
Contact information
Press contact
Julia Schnelldorfer
+49 162 2166891
julia.schnelldorfer@xpublisher.com
About Business Wire
For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Samsung Bioepis Announces Positive Preliminary Phase 1 and Phase 3 Data for SB27, a Proposed Biosimilar to Keytruda (Pembrolizumab)29.6.2026 10:19:00 EEST | Press release
Samsung Bioepis Co., Ltd. announced today that the Phase 1 and Phase 3 studies on SB27, a proposed biosimilar to Keytruda1 (pembrolizumab), have met their primary endpoints. “We are excited to announce preliminary results from the Phase 1 and Phase 3 studies for SB27, our pembrolizumab biosimilar candidate. These topline positive results reinforce our scientific expertise and leadership in biosimilar development,” said Donghoon Shin, Executive Vice President and Head of Clinical Sciences Division at Samsung Bioepis. “We are on track to complete both Phase 1 and Phase 3 studies within this year. Leveraging our robust quality management system, we remain committed to advancing our biosimilar portfolio to broaden access to life-saving biologic medicines for patients with unmet needs.” Pembrolizumab is a humanized monoclonal antibody that acts as an immune checkpoint inhibitor by targeting and blocking the programmed cell death protein 1 (PD-1) receptor on T cells. It is used to treat vari
IQM Named a Major Player in the IDC MarketScape: Worldwide Quantum Computing 2026 Vendor Assessment29.6.2026 10:00:00 EEST | Press release
IQM today announced it has been named a Major Player in the IDC MarketScape: Worldwide Quantum Computing 2026 Vendor Assessment. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260629748732/en/ IQM named a major player in the IDC MarketScape IQM believes this recognition comes as institutions worldwide move quantum computing out of shared cloud access and into infrastructure they own and operate themselves. IQM calls this Production Quantum: full-stack, open-architecture superconducting systems deployed on premises, inside customers' own data centers and HPC environments, where organizations own the hardware, build internal expertise, and run quantum processors alongside their existing classical infrastructure. According to the IDC MarketScape, "For institutions building long-term quantum programs, this means the workflows and intellectual property developed on IQM hardware remain portable." The report further advises: "Consi
Zambon Announces Positive CHMP Opinion for Hopledo® (IPX203) for Adults with Parkinson’s Disease and Moderate to Severe Motor Fluctuations29.6.2026 10:00:00 EEST | Press release
Zambon today announced that the Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending the granting of a marketing authorization by the European Medicines Agency (EMA) for Hopledo® (modified-release levodopa/carbidopa) for the treatment of adult patients with Parkinson’s disease and moderate to severe motor fluctuations who have not been sufficiently stabilized with oral levodopa/DDC inhibitor-based treatment regimens. CHMP recommendation is based on data from the Phase 3 RISE-PD trial, which compared Hopledo® with immediate release levodopa/carbidopa (LD/CD) formulation in patients with Parkinson’s disease and moderate to severe motor fluctuations. In the study, Hopledo® demonstrated a significant increase in Good ON time over immediate release LD/CD with fewer daily doses and a comparable safety profile1. Hopledo® is a first-in-class, oral, modified-release formulation of LD/CD designed for the treatment of fluctuations of Parkinson’s diseas
Enhertu ® Approved in the EU as First Tumor Agnostic HER2 Directed Therapy and Antibody Drug Conjugate for Patients with Previously Treated HER2 Positive Metastatic Solid Tumors29.6.2026 09:30:00 EEST | Press release
Enhertu® (trastuzumab deruxtecan) has been approved in the European Union (EU) as a monotherapy for the treatment of adult patients with unresectable or metastatic HER2 positive (immunohistochemistry [IHC] 3+) solid tumors who have received prior treatment and who have no satisfactory treatment options. Enhertu is a specifically engineered HER2 directed DXd antibody drug conjugate (ADC) discovered by Daiichi Sankyo (TSE: 4568) and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca (LSE/STO/NYSE: AZN). The approval by the European Commission follows the positive opinion of the Committee for Medicinal Products for Human Use of the European Medicines Agency and is based on results from subgroups of patients with HER2 positive (IHC 3+) tumors across three phase 2 trials, including DESTINY-PanTumor02, DESTINY-Lung01 and DESTINY-CRC02. In DESTINY-PanTumor02, Enhertu demonstrated a confirmed objective response rate (ORR) of 52.3% (95% confidence interval [CI]: 42.6-6
Beerenberg Prevails in Patent Case Against Aspen Aerogels29.6.2026 08:00:00 EEST | Press release
The Korean Patent Court has invalidated three of Aspen Aerogels’ patents related to improved hydrophobic aerogel material. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260628192007/en/ Beerenberg delivers high-end insulation solutions built for performance, reliability, and long-term value. (Photo: Beerenberg) The ruling confirms the conclusion of the Intellectual Property Trial and Appeal Board (IPTAB) that the patents did not meet the necessary requirements for patentability. Beerenberg, which specializes in high-end insulation products, welcomes the court’s decision. “We are pleased that the case has now been concluded and that any uncertainty regarding the infringement claims has been removed,” says CEO Arild Apelthun. About Beerenberg Beerenberg has delivered cost-efficient solutions to a wide range of industrial enterprises for 49 years. The company is one of the leading suppliers of maintenance and modification serv
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom