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Ratings and Reviews 0 Ratings
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What is studioMED+?
Germany stands at the forefront of research in Europe, undertaking more than 600 clinical and non-clinical studies annually. The complexity of managing these studies is increasing, necessitating meticulous coordination of appointments and personnel, prompt updates of study data, and straightforward access to documents for inquiries. It's essential to move away from the constraints of a paper-based system; by opting for a lightweight tablet, you can access information in seconds, allowing you to focus on what truly drives progress in your research. The digital study management solution offered by studioMED+ is crafted to assist you in making this vital transition. No matter where you are or what time it is, studioMED+ provides a flexible tool that effortlessly adapts to your unique requirements, ensuring your research process remains both efficient and effective. By embracing this innovative solution, you will not only enhance your productivity but also position yourself at the cutting edge of study management advancements. Make the switch today and witness how streamlined processes can transform your research endeavors.
What is QuesGen Platform?
We offer a diverse array of solutions that range from simple turnkey systems to comprehensive multi-site research initiatives, aiding principal investigators in overcoming common issues related to database selection and configuration. Researchers often seek out QuesGen for specialized advice on the best practices for data management and additional services that help expedite the commencement of their research studies. As a trusted partner for a variety of academic institutions and researchers, we are adept at managing large datasets and performing data curation through our versatile data platform, which supports the quick and efficient launch and scaling of research projects. Our extensive data model, along with a repository of assessments and curation expertise, reflects QuesGen's commitment to getting you operational in no time while ensuring the delivery of high-quality, compliant data that allows you to focus on analyzing your results. Our offerings cater to a wide range of clinical research activities within your organization, conforming to HIPAA regulations and FDA 21 CFR Part 11 standards, and they can be effortlessly integrated with your electronic medical records systems as well as the Federal Interagency TBI Repository (FITBIR). By utilizing our services, researchers can not only improve their efficiency but also enhance their workflows, ultimately contributing to more significant and impactful research results, while fostering a collaborative environment that encourages innovation and discovery.
Integrations Supported
Additional information not provided
Integrations Supported
Additional information not provided
API Availability
Has API
API Availability
Has API
Pricing Information
$200 per month
Free Trial Offered?
Free Version
Pricing Information
$100 per month
Free Trial Offered?
Free Version
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
studio.201 software
Date Founded
2019
Company Location
Germany
Company Website
www.studiomedplus.de
Company Facts
Organization Name
QuesGen Systems
Date Founded
2004
Company Location
United States
Company Website
www.quesgen.com
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
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