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Dec 17, 2025, 09:32 ET LILEE Systems Advances Mission-Critical Train Control Interoperability in the Northeast Corridor
testing, demonstrations, training, and warranty following final acceptance. LILEE will also support documentation for PTC Safety Plan updates under 49 CFR Part 236.1033, ensuring CMU compliance with federal safety requirements."Achieving true interoperability between different STS systems is a regulatory
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Dec 17, 2025, 08:30 ET Baird Medical Establishes U.S. Manufacturing Base to Accelerate Global Expansion and Future R&D
sq ft temperature-controlled warehouse. The facility is both FDA registered and ISO certified. MPS's is certified to ISO 13485 standards, US FDA 21 CFR Part 820 Quality System regulations and ISO 14971 Medical Device, Risk Management standards.Forward-Looking StatementsThis press
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Dec 15, 2025, 10:15 ET Pharmaceutical Manufacturing Execution System Market worth $4.62 billion by 2030 - Exclusive Report by MarketsandMarkets™
pressures, the need for end-to-end batch visibility, and the rapid shift toward digitalized, paperless manufacturing. Regulatory frameworks such as FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and global GMP standards are compelling pharmaceutical companies to adopt MES to ensure data integrity, electronic batch
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Dec 10, 2025, 11:28 ET CXZONE VON ACTO ERHÄLT ZWEI AUSZEICHNUNGEN BEI DEN 2025 PHARMACEUTICAL TECHNOLOGY EXCELLENCE AWARDS
Frontlinie den Einblick geben, den sie benötigen, um die Effektivität des Außendienstes kontinuierlich zu steigern. Als validierte Plattform, die mit FDA 21 CFR Part 11 konform und SOC 2 Typ II-zertifiziert ist, ist ACTO der zuverlässige Partner für intelligente Spitzenleistungen in der Life-Science-Branche.
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Dec 09, 2025, 15:37 ET DOUBLE DISTINCTION POUR CXZONE D'ACTO AUX PRIX D'EXCELLENCE 2025 PHARMACEUTICAL TECHNOLOGY
ligne les informations dont ils ont besoin pour assurer l'efficacité continue des équipes de terrain. Plateforme validée conforme à la norme FDA 21 CFR partie 11 et certifiée SOC 2 Type II, ACTO est le partenaire de confiance pour des renseignements d'excellence sur le terrain dans le secteur des sciences
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Dec 09, 2025, 15:36 ET CxZone de ACTO gana doble distinción en los Premios a la Excelencia en Tecnología Farmacéutica 2025
primera línea la información necesaria para impulsar la eficacia continua de su equipo de campo. Como plataforma validada que cumple con la norma 21 CFR Parte 11 de la FDA y cuenta con la certificación SOC 2 Tipo II, ACTO es el socio de confianza para la excelencia inteligente de campo en la industria
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Dec 09, 2025, 08:30 ET ACTO'S CXZONE WINS DUAL HONORS IN THE 2025 PHARMACEUTICAL TECHNOLOGY EXCELLENCE AWARDS
leaders and frontline managers with the insight they need to drive continuous field force effectiveness. As a validated platform compliant with FDA 21 CFR Part 11 and SOC 2 Type II certified, ACTO is the trusted partner for intelligent field excellence in the life sciences industry.
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Dec 09, 2025, 08:30 ET ACTO'S CXZONE WINS DUAL HONORS IN THE 2025 PHARMACEUTICAL TECHNOLOGY EXCELLENCE AWARDS
leaders and frontline managers with the insight they need to drive continuous field force effectiveness. As a validated platform compliant with FDA 21 CFR Part 11 and SOC 2 Type II certified, ACTO is the trusted partner for intelligent field excellence in the life sciences industry.
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Dec 09, 2025, 06:30 ET Bio-Techne Launches the Enhanced Leo™ System Delivering Advanced Multiplexing and High-Throughput Protein Analysis
supports complex assay configurationsStrengthens Bio-Techne's leadership in proteomic analytical instruments and supports 21 CFR Part 11 complianceMINNEAPOLIS, Dec. 9, 2025 /PRNewswire/ -- Bio-Techne
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Dec 02, 2025, 09:30 ET Dickson Launches Mapping Suite for Global Markets
studies.Seamless Regulatory Compliance: Mapping Suite meets the highest health and industry standards including GxP, WHO, FD X 15-140, 21 CFR Part 11 and EU Annex 11 without sacrificing efficiency.Validation Made Simple: Optional IQ/OQ (Installation Qualification/Operational
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Dec 02, 2025, 09:05 ET Flywheel Launches Validated Imaging Solution to Accelerate Decision-Making Across the Clinical Trial Ecosystem
improve data access for clinical trial stakeholders. Flywheel Validated (a specific version of Flywheel's core technology platform) is compliant with 21 CFR Part 11, helping organizations conducting regulated or near-regulated trials and AI model development accelerate time-to-decision and time-to-market.
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Dec 02, 2025, 06:42 ET Prefilled Syringes (PFS) Market Size to Grow USD 32.98 Billion by 2035 at a CAGR 13.75 | Vantage Market Research
Leadership in biologics manufacturing, strong uptake of safety syringes, advanced fill-finish technologies, and high regulatory compliance standards (FDA 21 CFR Part 820, USP <1207>).Europe: Largest hub for prefilled syringe production; strong adoption in vaccination programs, chronic disease
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Dec 01, 2025, 13:15 ET S&P Global Energy Celebrates Ten-year Anniversary of Platts Benchmark Steel Rebar and Scrap Assessments as Settlement Basis for London Metals Exchange
contracts with settlement against the Platts benchmark for spot physical premium steel scrap delivered to Turkey on a cost and freight (CFR) basis, known as Platts HMS 1/2 80:20 CFR Turkey* benchmark, and the Platts spot physical steel rebar benchmark, known as Platts Steel Rebar free-on-board (FOB) Turkey,
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Dec 01, 2025, 07:00 ET Anju Software Unveils Luminee, the AI Engine That Builds Validated EDC Databases in Days -- Winner of SCOPE EU 2025 Innovation Award
expectationsIntegration across Anju's eClinical ecosystem, including TrialMaster and TrialBuilderImproved data quality and compliance, aligned with 21 CFR Part 11, GCP, HIPAA, and GDPRLuminee is available from Anju Clinical, giving data managers, clinical operations teams, and research organizations
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Nov 27, 2025, 03:58 ET Happiest Minds Launches ELAIRA, an Intelligent Digital Co-Worker for Enterprise Support
multi-step workflows leveraging Agentic AI. Designed specifically for regulated environments, ELAIRA adheres to pharma-grade standards including GxP, 21 CFR Part 11, EU Annex 11, and ALCOA+. Leaders gain real-time visibility into SLA performance, compliance posture, and value metrics through a unified dashboard
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Nov 25, 2025, 08:42 ET REACH Trial and The Concinnity Company™ Collaborate to Enhance Investigator-Initiated Trial Oversight with Cloud Concinnity®
CEO, The Concinnity CompanyAbout The Concinnity CompanyThe Concinnity Company is the creator of Cloud Concinnity, a secure, 21 CFR Part 11 validated process integration and automation platform purpose-built for clinical trial oversight and broadly applicable to any workflow-driven
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Nov 20, 2025, 08:32 ET RealTime eClinical Solutions Ends Duplicate Data Entry from eSource to EDC with Launch of EDC Connect
EDC Connect aligns RealTime-eSource with leading third-party EDC systems, offering unmatched flexibility while maintaining full compliance with 21 CFR Part 11 standards. As part of RealTime's unified Site Operations Management System (SOMS), EDC Connect reinforces the company's
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Nov 15, 2025, 13:48 ET Notizie di Artmarket.com: Artprice lancia Artprice News, la prima agenzia di stampa al mondo interamente dedicata all'arte e al suo mercato, disponibile in 11 lingue e 122 paesi, insieme a Cision PR Newswire e Perplexity AI
Artprice sono stati fondati nel 1997 da thierry Ehrmann, amministratore delegato dell'azienda. Sono controllati dal Groupe Serveur (creato nel 1987). cfr. la biografia certificata di Who's Who In France©:
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Nov 14, 2025, 08:53 ET SAS Clinical Acceleration debuts to modernize clinical trials and accelerate time to market
Regulatory compliance & data security: SAS Clinical Acceleration supports compliance with the FDA's Title 21 CFR Part 11 requirements via audit trails, electronic signatures, versioning and role-based privileges. It also supports CDISC and its initiatives – dataset-JSON
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Nov 13, 2025, 09:00 ET Domino Data Lab Accelerates Statistical Programming and Submissions with Audit-Ready Traceability
eliminates duplicate effort and enforces proper sequencing while supporting dual-programmer validation to maintain complete traceability aligned with 21 CFR Part 11. Centralizing QC tracking and documentation within the SCE creates a single, trusted source of record for all analytical
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Nov 12, 2025, 16:54 ET INTEGRA REPORTS THIRD QUARTER 2025 RESULTS; STRONG PRODUCTION FROM FLORIDA CANYON MINE, RECORD ADJUSTED NET EARNINGS, AND IMPROVED FINANCIAL POSITION
Federal and State agencies early in 2025. In a letter dated August 19, 2025, the BLM notified Integra that the MPO met the content requirements at 43 CFR 3809.401(b), and thus was determined to be administratively complete. The BLM, its third-party National Environmental Policy Act ("NEPA") consultant,
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Nov 10, 2025, 16:39 ET Grand Teton mountain-runner pardoned; Fior documentary slated for 2026
34s. On Sep. 2, 2025, a year to the date of Michelino's record, the Yellowstone Justice Center found him guilty of violating 36 CFR § 2.1(b). But, on the eve of Michelino's sentencing hearing, DOJ reversed course, offering to dismiss the case after 60 hours of community service and
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Nov 10, 2025, 11:13 ET Medicom Now Fully Contracted with 17 of 18 VA Regions, Announces New VISN 10 and 17 Agreements
Required Disclosures In compliance with CFR § 852.203-70, Medicom declares that statements made herein do not imply that the Department of Veterans Affairs approves or endorses the Contractor's
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Nov 05, 2025, 13:38 ET ACTO STELLT ACTOVERSE VOR: EIN MARKTPLATZ FÜR PARTNERLÖSUNGEN ZUR FÖRDERUNG VON INNOVATION UND EFFIZIENZ IM BEREICH EXZELLENZ AUF DEM VEEVA COMMERCIAL SUMMIT EUROPE
Frontlinie den Einblick geben, den sie benötigen, um die Effektivität des Außendienstes kontinuierlich zu steigern. Als validierte Plattform, die mit FDA 21 CFR Part 11 konform und nach SOC 2 Typ II zertifiziert ist, ist ACTO der zuverlässige Partner für intelligente Außendienst-Exzellenz im Bereich der Biowissenschaften.
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Nov 05, 2025, 13:35 ET ACTO DÉVOILE ACTOVERSE : UN MARCHÉ DE SOLUTIONS PARTENAIRES FAVORISANT L'INNOVATION ET L'EFFICACITÉ DANS L'EXCELLENCE OPÉRATIONNELLE AU VEEVA COMMERCIAL SUMMIT EUROPE
informations dont ils ont besoin pour favoriser l'efficacité continue des forces de terrain. En tant que plateforme validée conforme à la norme FDA 21 CFR Part 11 et certifiée SOC 2 Type II, ACTO est le partenaire de confiance pour l'excellence intelligente sur le terrain dans l'industrie des sciences de
More news about: ACTO Technologies, Inc.