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Ratings and Reviews 2 Ratings
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StrivenStriven is the complete business management solution that cuts your costs, optimizes your processes, and makes daily tasks simpler. Transform your company's data into something unified, interconnected, and meaningful. Drawing on over two decades of Software Services expertise, we've worked alongside more than 8,600 organizations spanning dozens of sectors to make their operations more secure, productive, and valuable for their customers. Empowering people to accomplish more has always driven us. Now, it's central to our software design. We feature simple, transparent pricing plans and an exceptional guarantee. You can even start using it immediately at zero cost. Our plans come with no trial periods, expiration dates, or contractual commitments.
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CapitalcoreCapitalCore serves as an online brokerage that facilitates Forex (CFD) and binary options trading, boasting some of the most competitive payouts in the market. Our platform grants access to a variety of global currency pairs for CFD trading and offers straightforward, rapid binary options. Traders can take advantage of prompt withdrawals, narrow spreads, and robust trading tools designed for optimal performance. With a diverse selection of account types and personalized support, we strive to assist traders at all experience levels in reaching their financial aspirations. At CapitalCore, we focus on providing a smooth trading journey by presenting an intuitive interface, rapid trade execution, and up-to-the-minute market data. Our sophisticated analytical tools and indicators enable traders to make informed decisions confidently. Whether you favor manual trading techniques or automated approaches, our platform accommodates all trading preferences. We also emphasize the safety of client funds through top-notch encryption, secure payment options, and negative balance protection, ensuring peace of mind for our users. Furthermore, we provide our clients with a wealth of educational materials that include market insights, daily analyses, webinars, and expert trading tactics to refine their abilities. Our dedicated multilingual customer support team is available around the clock to address any questions, thereby guaranteeing a seamless and effective trading experience for everyone involved. Ultimately, we aim to foster a vibrant trading community where individuals can thrive and achieve their financial goals.
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RegDeskRegDesk stands out as the leading RIMS platform enhanced by AI, tailored specifically for Medical Device, Pharmaceutical, and IVD companies. • Our unique Regulatory Intelligence encompasses data from over 120 countries, all presented in a uniform format, and includes timely alerts regarding regulatory updates. • With our AI-driven Application Builder, regulatory affairs teams can efficiently create and submit global applications in a fraction of the usual time. • The Change Assessment feature enables RA teams to evaluate the implications of changes on current products and determine the necessary actions. • Our Distributor Collaboration tool facilitates smooth workflows for communication and document sharing with external partners. • The Standards Management function simplifies the process for RA teams to locate and oversee both international and country-specific standards. • Additionally, our Tracking & Reporting capability empowers teams to monitor regulatory initiatives worldwide, receive notifications for renewals, and quickly compile reports on key performance indicators. To learn more about our offerings, please explore our website.
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QualioQualio is a unified quality and compliance platform that helps growing life sciences companies scale faster while staying continuously audit- and inspection-ready. Medical device, digital health, biotech, and pharma teams use Qualio to replace manual processes and disconnected tools with a single source of truth for quality, regulatory readiness, and risk. With a modern eQMS at the foundation and Compliance Intelligence layered on top, Qualio moves teams beyond point-in-time audits. Automated gap analysis, cross-standard evidence mapping, and real-time readiness dashboards provide confidence that the organization is prepared today—not just when auditors arrive. Qualio centralizes document control, training, CAPA, change management, supplier quality, and design controls, linking them directly to regulatory requirements and product lifecycle data. Executive-ready views show compliance health by standard, region, and product, turning regulatory readiness into a measurable business capability instead of a black box. Compliance Intelligence continuously monitors for risk, highlights gaps early, and prioritizes remediation so teams focus effort where it matters most. Pre-validated regulatory frameworks are maintained as requirements evolve, reducing reliance on consultants and avoiding duplicate work as companies expand. The result is faster market entry, lower compliance cost, reduced risk of findings or recalls, and confident, risk-managed growth.
What is meddevo?
Meddevo provides a dedicated workspace for each team member, allowing them to create, manage, and automate the technical documentation related to medical devices and in vitro diagnostics (IVDs), functioning as a comprehensive SaaS solution. You can efficiently handle changes, Corrective and Preventive Actions (CAPAs), complaints, and tailored processes directly within the platform. Thanks to the seamless synchronization of the electronic Quality Management System (eQMS) and electronic Technical Documentation (eTD), you will achieve unparalleled visibility into your operations. This solution is designed to significantly decrease administrative workloads and streamline processing times, ultimately enhancing overall productivity. By leveraging these tools, teams can focus more on innovation rather than paperwork.
What is Greenlight Guru Clinical?
Medical device and diagnostics companies running clinical studies are often stuck configuring EDC software that was built for pharmaceutical trials and never designed around FDA, EU MDR, IVDR, or ISO 14155 requirements. Greenlight Guru Clinical solves that by being the only electronic data capture (EDC) system built from the ground up for medtech, so teams aren't reworking someone else's pharma template to fit a device study.
Designed exclusively for medtech, Greenlight Guru Clinical combines an easy to use clinical data platform with industry leading customer service, so teams generate reliable, compliant clinical data with confidence.
Get a single, validated platform covering the full lifecycle of a device or diagnostics study, including:
Electronic Data Collection and eCRF design, with GCP compliant structures and built in audit trails
ePRO/eCOA for patient and clinician reported outcomes, collected in person or remotely on any device
eConsent for compliant, auditable enrollment
Randomization (RTSM) for controlled and comparative studies
PMCF Surveys for post market clinical follow up under EU MDR
Adverse Events Reporting built into the platform
Leading-edge, open API for connecting study data to other clinical or quality systems
Greenlight Guru Clinical supports pre-market clinical investigations, post-market surveillance studies, registries, and human factors testing, and is used by both device and diagnostics manufacturers and by contract research organizations (CROs) that specialize in medtech. A validation package is included with every product update, removing the ongoing burden of software revalidation from the quality team. Every customer also gets a dedicated customer success manager with real medtech experience, not a generalist software account rep. For manufacturers already on Greenlight Guru's quality management system (QMS), Clinical extends into one connected platform spanning quality, product development, and clinical evidence.
Integrations Supported
BSI CTMS
ChatGPT
Claude
Cursor
Gemini
Medidata
Microsoft Excel
Oracle Clinical One
Prelude EDC
Tremendous
Integrations Supported
BSI CTMS
ChatGPT
Claude
Cursor
Gemini
Medidata
Microsoft Excel
Oracle Clinical One
Prelude EDC
Tremendous
API Availability
Has API
API Availability
Has API
Pricing Information
249€/User
Free Version
Free Trial Offered?
Pricing Information
Pricing not provided
Free Version
Free Trial Offered?
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
dytab GmbH
Date Founded
2018
Company Location
Germany
Company Website
www.meddevo.com
Company Facts
Organization Name
Greenlight Guru
Date Founded
2013
Company Location
Denmark
Company Website
www.greenlight.guru/clinical-electronic-data-capture-software
Categories and Features
Enterprise Content Management (ECM)
Archiving & Retention
Collaboration Tools
Content Lifecycle Management
Digital Asset Management
Document Management
Electronic Signature
Information Governance
Mobile Access
Search
Version Control
Workflow Management
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning
Electronic Data Capture
Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management