Audience

Pharmaceutical and medical device organizations seeking a solution to control and optimize their master data assets

About Chronicles CTMS

Full cycle product for Research and Development teams in Pharmaceutical Industry. The product includes Electronic Trial Master File, Trial Management, Electronic Document Management with eSignature support. That is suitable for regulated areas as it is fully compliant with 21CFR Part 11 requirements. We develop and support systems from the very begining to the ready-to-use product using modern agile methodology and feedback given by clients. Satisfaction of customers needs is our main concern. We provide automation services of quality management systems starting from SOPs development and training to systems integration and business processes adapation. Our personnel have expertise in GCP, GLP, GCLP and also have been involved in many research organizations' audits and software development. By purchasing the system you get the full package of documents, training and support. So you can focus on your business and delegate us all the technical issues.

Flex Databases
Flex Databases
(3 Ratings)
Flex Databases is an innovative, unified and compliant eClinical platform, providing software solutions for clinical trials: CRO and pharmaceutical companies. Our system consists of : - Clinical Trial Management System, - electronic Trial Master File - Project Management & Budgeting solution, specifically tailored for clinical trials industry - Pharmacovigilance system - Learning Management System Our unique experience and qualified team of over 100 professionals who possess a deep understanding of the clinical trial process made it possible to create a flexible platform.
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IBM Clinical Development
IBM Clinical Development
IBM® Clinical Development provides pharmaceutical, contract research organizations and medical device companies unified technology from start up to submission to support clinical trials. With our clinical data management system, users can organize and analyze report data from anywhere in the world. Enabling pharmaceutical organizations to deliver therapies faster to their patients. Design and launch studies without database migration. Deliver quick and easy remote consent with minimal integration.
Learn more
OpenText for Life Sciences
OpenText for Life Sciences
OpenText™ Information Management solutions help life sciences organizations leverage insights from data and content to improve decision-making processes and accelerate product development. Integrate, manage, and securely exchange data across people, systems and things. Leverage information assets from R&D to commercialization. Freedom of choice with cloud-native software that can run anywhere. OpenText for life sciences accelerates the discovery process by extracting actionable insights that drive pipeline innovation. Capture and manage research papers into electronic lab notebooks with intelligent capture. Find insights with text mining. Extract knowledge trapped in the unstructured text contained in clinical trial reports, study protocols, clinical safety and efficiency findings. Find out how to intelligently analyze, classify and extract clinical trial documents to reduce the risk of costly stops and starts.
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QureClinical
QureClinical
As a Data Management provider we offer data management and statistical analysis planning and model development with applicable CRF design. All the appropriate documentation is provided by us according to FDA and other regulations. Previous experience has shown us that putting more effort into the planning phase will give a better, faster and efficient result in the end-phase of the trial. Our databases are generated by experienced data managers who have worked with several eCRF-s and already know the critical parts of the electronic data capture system design and data collection. This allows the eCRF to be built in a short period of time. eCRF validation and testing is compulsory part of the design and is dealt by different personnel in order to receive a hundred-percent elaborated eCRF.
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Integrations

No integrations listed.

Ratings/Reviews - 1 User Review

Overall 5.0 / 5
ease 4.0 / 5
features 4.0 / 5
design 3.0 / 5
support 4.0 / 5
More Reviews Write a Review

Company Information

Chronicles Research Team
United States
inchronicles.com

Videos and Screen Captures

Chronicles CTMS Screenshot 1
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Product Details

Platforms Supported
SaaS

Chronicles CTMS Frequently Asked Questions

Q: What kinds of users and organization types does Chronicles CTMS work with?
Q: What languages does Chronicles CTMS support in their product?

Chronicles CTMS Product Features

Clinical Trial Management

Monitoring
21 CFR Part 11 Compliance
Electronic Data Capture
Enrollment Management
Patient Database
HIPAA Compliant
Document Management
Scheduling
Recruiting Management
Study Planning

Chronicles CTMS Reviews

Write a Review
  • A Chronicles CTMS User
    QA
    Used the software for: 1-2 Years
    Frequency of Use: Daily
    User Role: Deployment
    Company Size: 1 - 25
    Design
    Ease
    Features
    Pricing
    Support
    Probability You Would Recommend?
    1 2 3 4 5 6 7 8 9 10

    "Good solution for CTMS process automation"

    Posted 2021-11-29

    Pros: Easy, simple to start and reliable solution, with some not an ideal design, but does it`s tasks well.
    Added for us some small functionality by our request without additional pay.
    Good solution to start with eTMF and electronic documents templates for a tiny pricing scheme.
    Free updates with new features.

    Cons: Not ideal for its design and have some more functions to do, e.g. more easier templates customization.

    Overall: Good for its functions, support and price. Vendor are actively developing, so some functions are working with only simple customizations, but it's usually fixed in next releases. Hope it will grow up well, keeping updates for free as it was declared.

    Read More...
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