FABASOFT-APPROVE
17.1.2023 14:10:37 CET | Business Wire | Press release
Primetals Technologies relies on Approve on Fabasoft PROCECO for traceable communication with customers and manufacturers. In large projects lasting up to three years, as many as 50,000 documents belonging to the plant documentation (as-built documentation) have to be exchanged securely.
Approve supports the group's “transmittal management”, i.e. the contract-relevant communication involved in the coordination of technical documents between the project management and its partners. A direct data connection to SAP P&E (Projects & Engineering Support) replaces multi-stage transmission steps via internal drives and avoids manual effort. “With Approve, we have discovered a state-of-the-art, highly customizable platform for exchanging technical documents with our customers, suppliers, and internal project members”, explains Gerhard Guger, Head of Project Coordination Casting & ESP at Primetals Technologies. For each shipping package, a structured representation of the complex content is available to users directly in the cloud-based environment.
Secure data storage and compliance
The pioneer in plant equipment attaches great importance to data security when dealing with sensitive business data and protected know-how. With data storage in Austria and a highly secure, certified technological basis, the software meets these requirements to the full. “As a secure customer portal, Approve provides project management with a transparent and extremely user-friendly environment for transferring sensitive documents. The structured view of project documents and an intelligent search function make it easier to work with large volumes of documents and ensure traceability throughout the entire duration of the project,” adds Andreas Dangl, Managing Director of Fabasoft Approve.
More detailed information in this context can be found in the case study “Efficient transfer of as-built documentation”
About Fabasoft Approve
Fabasoft Approve GmbH is a European software provider for technical data and document management in the industrial sector. Thanks to the simple adaptability via no-code/low-code, customer-specific requirements can be implemented in no time at all. The digitalization company focuses on use cases in quality management, technical documentation and transmittal management. Cross-company processes link internal and external project partners on a common platform and digitally map the entire information life cycle for industrial products. Numerous major international companies rely on the cloud-based product Approve on Fabasoft PROCECO as a “single source of truth” in their digitalization strategy.
About Primetals Technologies
Based in London, Primetals Technologies is a technological pioneer and a leading global company in the fields of engineering, plant construction and lifecycle services for the metals industry. The joint venture of Mitsubishi Heavy Industries and partners employs approximately 7,000 people worldwide.
For additional information, visit the Fabasoft Approve Press Room, www.fabasoft.com/approve, or follow us on LinkedIn and Twitter @Fabasoft.
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/20230117005049/en/
About Business Wire
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
Incyte Announces Positive CHMP Opinion for Opzelura® (ruxolitinib) Cream for the Treatment of Adults with Moderate Atopic Dermatitis26.6.2026 13:30:00 CEST | Press release
If approved, Opzelura® (ruxolitinib) cream will be the first steroid-free, topical JAK treatment option in the European Union (EU) for adults with moderate atopic dermatitis (AD) for whom standard topical therapies have failedAD, the most common type of eczema which affects 230 million people globally,1 is a chronic, recurring, inflammatory and highly pruritic (itchy) skin condition that can have a significant impact on daily life2Phase 3 TRuE‑AD4 data supporting the positive CHMP opinion demonstrated that ruxolitinib cream met both co‑primary endpoints at Week 8, maintained disease control with as-needed treatment through Week 24 and was well tolerated3,4,5 Incyte (Nasdaq: INCY) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a positive opinion recommending the approval of Opzelura® (ruxolitinib) cream for the treatment of moderate atopic dermatitis (AD) in adult patients for whom topical corticosteroids
Datroway® Recommended for Approval in the EU by CHMP as First-Line Treatment for Patients with Metastatic Triple Negative Breast Cancer Who Are Not Candidates for Immunotherapy26.6.2026 13:00:00 CEST | Press release
Recommendation based on TROPION-Breast02 phase 3 trial where Daiichi Sankyo and AstraZeneca’s Datroway showed a statistically significant and clinically meaningful improvement for the dual primary endpoints of overall survival and progression-free survival If approved, Datroway has potential to be the first TROP2 directed antibody drug conjugate for patients in EU with a demonstrated overall survival benefit as first-line treatment Datroway® (datopotamab deruxtecan) has been recommended for approval in the European Union (EU) as monotherapy for the first-line treatment of adult patients with unresectable or metastatic triple negative breast cancer (TNBC) who are not candidates for PD-1/PD-L1 inhibitor therapy. Datroway is a specifically engineered TROP2 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 Committee for Medicinal Products for Human Use
DAYBU®(trofinetide) Recommended for Approval in the European Union by CHMP26.6.2026 12:49:00 CEST | Press release
-- European Commission decision expected in the coming months-- If approved, DAYBU®would become the first treatment for neurobehavioral symptoms of Rett syndrome in the European Union Acadia Pharmaceuticals Inc. (Nasdaq: ACAD) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion following a re-examination procedure, recommending the granting of a marketing authorization for DAYBU® (trofinetide) for the treatment of neurobehavioral symptoms of Rett syndrome in adults and pediatric patients aged five years and older. If granted marketing authorization by the European Commission, DAYBU® would be the first therapy approved for this indication in the European Union (EU). “The CHMP’s positive opinion for DAYBU® is an important milestone in our mission to bring this innovative therapy to the EU, where there are no therapies specifically approved for the neurobehavioral symptoms of this devastating
HTEC Showcases Lakebase Branching at Databricks’ Data & AI Summit26.6.2026 11:18:00 CEST | Press release
HTEC, the global technology and AI engineering firm headquartered in Silicon Valley, last week showcased how it used Lakebase data branching to enable faster development, safer operations, and new possibilities for data-driven organizations operating in highly regulated environments. The Solution was developed in collaboration with a leading risk and compliance technology provider who serves financial institutions. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260626875859/en/ HTEC, the global technology and AI engineering firm headquartered in Silicon Valley, last week showcased how it used Lakebase data branching to enable faster development, safer operations, and new possibilities for data-driven organizations operating in highly regulated environments. Solving Critical Development Bottlenecks in Regulated Environments At the core of the collaboration was a shared challenge: how to enable modern data workflows in an envi
Stallergenes Greer Named One of Switzerland’s Best Managed Companies for 202626.6.2026 10:28:00 CEST | Press release
Stallergenes Greer, a global leader in allergy care, has been recognised for its overall business performance, company culture, and sustained growth by receiving the prestigious 2026 Switzerland’s Best Managed Companies award. The 2026 Best Managed Companies programme award winners are among Switzerland’s best private companies. The awards are derived from Deloitte’s global Best Managed Companies awards programme, an internationally recognised programme that evaluates businesses based on their leadership in the areas of strategy, culture and commitment, capabilities, innovation, governance and financial performance. Applicants are evaluated by an independent jury of experts. The evaluation of the Switzerland awards is based on more than 30 years of observed practice from the global awards programme that has been rolled out in 50+ countries worldwide. This recognition reflects Stallergenes Greer's consistent ability to deliver on its strategic vision while maintaining the operational di
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