Clienvo eTMF

Clienvo eTMF

Clinevo
PvEdge

PvEdge

Sarjen Systems
+
+

Related Products

  • Qualio
    912 Ratings
    Visit Website
  • SciSure
    299 Ratings
    Visit Website
  • HR Partner
    205 Ratings
    Visit Website
  • Aesthetic Insight
    10 Ratings
    Visit Website
  • Sovos
    99 Ratings
    Visit Website
  • RegDesk
    19 Ratings
    Visit Website
  • SDS Manager
    4 Ratings
    Visit Website
  • OrangeHRM Advanced
    333 Ratings
    Visit Website
  • Predict360
    18 Ratings
    Visit Website
  • pCloud Business
    189 Ratings
    Visit Website

About

Clinevo electronic Trial Master File (eTMF) is an easy-to-use electronic Trial Master File in electronic (digital content) format for organizing and storing documents, images, and other digital content of clinical trials. Clinevo electronic Trial Master File (eTMF) has an inbuilt DIA reference model and meets regulatory guidelines. Clinevo MICC Intake is a web-based tool for Medical Information Call Center (MICC) and PV users to Log, Track and Monitor Product Quality Complaints (PQCs), Medical inquiries (MIs) and Adverse Events (AEs). Clinevo Safety is a cloud-based, user-friendly, easy-to-use, regulatory-compliant end-to-end Pharmacovigilance / Drug safety system. The All-in-one system provides PV Intake, Case Processing, Regulatory Submissions / AS2 Gateway, Analytics, and Safety signals capabilities under one platform. Clinevo Website Intake is a web-based tool which can be connected to Sponsor / CRO websites to provide Consumers and Reporters a User friendly web interface.

About

PvEdge is a cloud-ready pharmacovigilance software designed to provide end-to-end compliant safety solutions for drugs, devices, vaccines, and combination products. It offers a comprehensive safety database that manages pharmacovigilance intake, case processing, submissions, AI & analytics, and safety signals all in one platform. The system adheres to existing and upcoming regulations, such as 21 CFR Part 11, ANNEX 11, GxP, and GDPR, ensuring global compliance. PvEdge utilizes advanced automation powered by AI and machine learning algorithms to enhance efficiency in drug safety database management. Key features include automated literature monitoring, ICSR submissions, smart triage, automated signal detection, and document automation. The platform also provides a controlled document management system for creating, managing, and publishing pharmacovigilance documents, as well as a risk-based enterprise quality management system to implement quality processes and training records.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Organizations seeking a clinical trial management solution

Audience

Pharmaceutical companies and healthcare organizations seeking solution to manage pharmacovigilance activities, ensuring compliance

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

No information available.
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 5.0 / 5
ease 5.0 / 5
features 5.0 / 5
design 5.0 / 5
support 5.0 / 5

Reviews/Ratings

Overall 5.0 / 5
ease 5.0 / 5
features 5.0 / 5
design 5.0 / 5
support 5.0 / 5

Pros & Cons from Real Users

Pros

  • The platform is simple & easy to use. Documents are pretty easy to search. The software comes with a prebuilt DIA reference model. It provides advanced analytics to track Completeness, Quality, Timeliness. The best feature is this platform can be easily integrated with CDMS/ CTMS systems. It also has the feature of uploading hundreds of documents in one go using a simple drag and drop.

Cons

  • Haven't found any problem till the date. So, no cons as Such.

Pros & Cons from Real Users

Pros

  • User-Friendly Interface – Easy to navigate, even for mid- to large-sized teams. Responsive Support Team – Actively listens to feedback and implements improvements. AI-Powered Modules – Automation in case intake, triage, and literature screening reduces manual workload and improves efficiency. Frequent Version Upgrades – Keeps the system aligned with evolving regulatory requirements. Easy Integrations – Smooth connectivity with regulatory gateways, third-party tools, and internal systems. Cost-Effective – Offers enterprise-level capabilities at a competitive price compared to larger vendors.

Cons

  • Initial Learning Curve – Advanced AI and automation features may require some initial training. Customization Time – Specific workflow customizations may take time depending on requirements. Dependence on Upgrades – Frequent updates require teams to stay aligned with new feature releases.

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

Clinevo
United States
www.clinevotech.com

Company Information

Sarjen Systems
Founded: 1998
India
pvedge.sarjen.com

Alternatives

Alternatives

Dialog

Dialog

Clarivate
Clinion eTMF

Clinion eTMF

Clinion
Thrana Safety Database

Thrana Safety Database

Thrana Softech
Clinevo Safety

Clinevo Safety

Clinevo Technologies

Categories

Categories

Integrations

No info available.

Integrations

No info available.
Claim Clienvo eTMF and update features and information
Claim Clienvo eTMF and update features and information
Claim PvEdge and update features and information
Claim PvEdge and update features and information