by Xybion

5 / 5 1 review

Who Uses This Software?

Pharmaceutical, biotech and CRO's

Average Ratings

1 review
  • Overall 5 / 5
  • Ease of Use 5 / 5
  • Customer Service 5 / 5
  • Features 4 / 5
  • Value for Money 5 / 5

Product Details

  • Starting Price $10000/one-time
  • Pricing Details Per user and server based
  • Free Version No
  • Free Trial No
  • Deployment Cloud, SaaS, Web
    Installed - Windows
  • Training In Person
    Live Online
  • Support Business Hours

Vendor Details

  • Xybion
  • Founded 1977

About Pristima

From handling simple to complex GLP and non-GLP compliant laboratory environments, Xybion's enterprise solution for pre-clinical data management solution, Pristima enables a significant reduction in time to final report and study close-out through full lifecycle automation. The Pristima suite offers numerous modules, which allow you to select a targeted combination of functions to meet your specific organizational requirements and workflows.

Pristima Features

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

Pristima Most Helpful Reviews

Preclinical software that delivers full life cycle automation, support for Research and Safety study

Translate with Google Reviewed on 7/21/2016
Sandeep V.
Market Intelligence Associate
Research, 201-500 Employees
Used the Software for: 2+ years
Reviewer Source 
Source: asdf
5 / 5
Ease of Use
4 / 5
Features & Functionality
5 / 5
Customer Support
5 / 5
Value for Money
Likelihood to Recommend:
Not Likely Extremely Likely

Pristima is a fully integrated enterprise solution for preclinical data management that delivers complete life cycle automation and support for Pharmacology and Drug Safety Research Study Management, Vivarium Management, and Veterinary Care. From breeding and ordering through the study submission process, the Pristima® Suite manages the planning and recording of data, controls authorized changes, and assembles the data for submission to regulatory agencies.

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