Dsg-us 代替案 & 競合他社
DSG offers a comprehensive fully integrated suite of EDC clinical trial and decentralized trial software, and data management services for all bio-tech and life sciences industries.
代替品と競合他社 dsg-us.com コンテンツ、トラフィック、構造に関して
Anju: Transforming Healthcare and Life Sciences. Explore our innovative solutions and industry expertise.
Clinion Makes Clinical Trials Faster, Easier and Better With its AI-enabled eClinical Platform. Explore How Clinion Can Accelerate Your Next Trial!
Acceliant – eClinical Solutions Designed For your Needs.
Plateforme unifiée de gestion du contenu et de l'information pour soutenir le développement des produits des sciences de la vie : Qualité, Clinique, Réglementaire, Pharmacovigilance, Commercial
SimpleTrials is an on-demand Clinical Trial Management System (CTMS) for sponsors, CROs and sites.
Clinitec - Interactive Voice Response, IVRS Systems, IWRS systems, Patient Randomisation, Patient Diaries, Drug Supply Management. Applications in Clinical Trials Management
Octalsoft is your trusted partner for electronic data capture Software & clinical trial solutions. Streamline your clinical research with Octalsoft's clinical trial Software.
Ivrsdevelopment.com is ranked number 10M in the world and links to network IP address 50.63.202.88.
4G Clinical supports trials of any phase and complexity with flexible randomization and trial supply management (RTSM) and supply optimization solutions.
Mednet’s comprehensive EDC-based eClinical platform provides flexible clinical trial solutions for all study types and phases.
Leverage our global, cloud-based technology for end-to-end, direct-from-source data collection and study management across all clinical trial phases.
The EvidentIQ offering brings an innovative end to end eClinical solution. We support 15 of the top 20 pharma companies through novel RWE solutions and +150 SMB customers in over 20 countries.
Whether as a sponsor, CRO or SMO – BSI life sciences software covers your specific processes and features. Our innovative software solutions for CTMS, eTMF and more are made in Switzerland, Germany and the USA.
Discover Engility® the cloud Clinical Trial Management System and integrated electronic trial master file CTMS eTMF
Explore DDi's comprehensive solutions for clinical, regulatory, and automation needs in the life sciences industry.
Manage your Clinical Supplies and your entire Clinical Trial efficiently and seamlessly using our integrated and modularized solutions.
SCOPE Europe, hosted on 29-30 October 2024, in Barcelona, Spain, gathers clinical innovation leaders, clinical operations executives, clinical trial managers, and more to discuss the planning and management of clinical trials in Europe and the rest of the world.
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Risk-Based Quality Management and Risk-Based Monitoring is simple with our RBQM technology, OPRA. For all clinical trial phases, used by global Sponsors and CROs, OPRA delivers end-to-end ICH E6(R2) compliant Quality Management. From critical factor identification, through risk assessment and management, and Central Monitoring through to one-click reporting. With TRI's training and clinical operations support OPRA will transform the way you run your clinical trials and improve your data quality.
Your All-In-One eClinical Software Platform
Clinevo Technologies, a software solution company specialized in ctms clinical trial, etmf software, and the leading pharmacovigilance companies in India, USA, Europe,etc.
SimpleCTMS is a web-based Clinical Trial Management System (CTMS).
We are a leading CaaS (Communication as a Service) provider, Voice, SMS, Secure Messaging and AI-driven conversational solutions customized for your business
Clinigen | A leading pharmaceutical services company accelerating access to medicines for patients in every corner of the globe.
Signant Health's science-backed technology solutions and supporting services optimize clinical trials to ensure accurate, reliable endpoints.
CIMS Global – Innovative Clinical Trial Solutions.
Prevail InfoWorks’ Single Interface is a single, role-based access point to everything drug development, for improved patient and study outcomes.
ResearchManager - Clinical Research Suite ✓ ISO 27001 & NEN 7510 gecertificeerd ✓ GCP & GDPR compliant ✓ Neem contact op!
Learn about the first and only holistic Regulatory Information Management (RIM) software for medical device companies that consolidates all the functions of regulatory affairs.
ComplyDocs eTMF is an affordable and powerful eTMF (electronic Trial Master File) software for clinical trials. Easy to use, quick to implement.
Freyr provides Regulatory Software, Automation and Digital Transformation Solutions to Lifesciences companies across the globe.
The S-Clinica Anticipatory Management Engine is the most advanced algorithm in the IRT RTSM industry for Clinical Supply forecasting, planning and management. The system manages any study design complexity in any study phase. It's delivered fast, can be introduced mid-study or for emergencies.
Advanced Drug Supply Chain Management and Clinical Trial Execution Technology
Arma Partners provides independent corporate finance advice to companies and investors active in the global digital economy. Contact our team today.
IRT, eConsent, and eCOA solutions to help you wisely guide novel science through complex clinical trials
CHI's 9th Annual Clinical Trial Innovation Summit, November 10-11, 2020, Boston, MA, is multi-track event on best practices needed to optimize clinical trial innovation, planning and management. Topics include feasibility & site selection, clinical data & technology, patient engagement & enrollment, risk-based monitoring, and budeting & clinical outsourcing.
Celebrating its 11th successful year, SCOPE Summit 2020 takes place February 18-21 in Orlando, FL. Over the course of four stimulating days of in-depth discussions in 20 different conferences, 3 plenary keynote sessions, the annual Participant Engagement Awards, and the ever-popular interactive breakout discussions, the programming focuses on advances and innovative solutions in all aspects of clinical trial planning, management and operations, including: Site Selection and Management, Patient Engagement, Recruitment and Retention, Protocol Optimization, Feasibility, Data Strategy and Analytics, Sensors and Wearables, Project Management, Outsourcing, Forecasting, Budgeting and Contracting, Resource Management, Quality (QbD) in Trial Conduct, Risk-Based Monitoring, Artificial Intelligence, Post-Marketing Studies, Observational Research, Accessing and Generating RWD, Clinical Biomarker Strategy, Clinical Supply Chain, Precision Medicine, Clinical Biomarkers and Biospecimens, and Central Lab Solutions, and an al
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