LIFESPHERE® SAFETY
LitPro
Intelligent automation for medical literature monitoring and assessment.
JUMP TO
Streamlining Literature Screening with Intelligent Automation.
A full-service, automated medical literature database screening solution designed to help life sciences organizations meet regulatory compliance requirements and improve pharmacovigilance processes with automation.vigilance processes with automation.
BENEFITS
Complete Literature Screening Solution
LifeSphere LitPro is easily configurable as medical literature monitoring searches change over time, helping to ensure compliance and future preparedness. LifeSphere LitPro automates the process of
- Identifying and retrieving all relevant journal article details from accessible bibliographic databases such as Embase and MEDLINE/PubMed, among others
- Scanning the selected information sources for pertinent safety information
- Assessing the attribution to determine if there is a relationship between an event and a medicinal product
- Recognizing and extracting key data points for use as part of the creation of an ICSR or follow-up report to an existing case within a safety database
Enables Highly Accurate Benefit-Risk Evaluations
With improved data available for assessment, organizations can conduct accurate benefit-risk evaluations of potential signals for products based on the discovered data and establish quality periodic safety reports.
Compliance Made Easy
Fulfills regulatory requirements by automating literature surveillance, event identification, data extraction and case creation. This automated process decreases manual intervention and frees up teams to focus on core tasks.
RESULTS
Delivering Real Results to a Global Client Base
80
%
Of Top 50 Biopharmas
80% of the top 50 biopharma companies are our clients
80
%
Efficiency Gains
80% potential efficiency gains driven by our Nava cognitive computing engine
30
%
Cost Savings
30% immediate cost savings potential via our advanced automation capabilities
100
%
Compliance
100% compliance with all present and upcoming regulatory standards
FACT SHEET
Automated Literature Monitoring
LifeSphere LitPro is the industry’s first and only automated literature screening solution that offers system-agnostic integration with other drug safety systems. LitPro complements any literature search tools already in place, offering additional functionality such as review and triage.
WHITEPAPER
Regional Pharmacovigilance Regulations: Challenges with Non-Harmonized Regulatory Expectations
With the increasing global awareness in safety reporting, the volumes of ADRs in MAH/national/global databases are also expected to increase at the same time. To derive meaningful insights from these huge volumes of safety data, it is important that the ADRs obtained from various sources are compiled and collated in a meaningful manner.
BLOG
ArisGlobal’s LifeSphere MultiVigilance 10 Helps SMBs Manage and Master Pharmacovigilance
Managing and Mastering Pharmacovigilance covers how LifeSphere Multivigilance 10 benefits small to medium-sized businesses by utilizing industry-standard practices and proper management processes.
PARTNERS
Partnering With the Industry’s Best
FEATURES
Improve Efficiency, Productivity, and Cost Savings.
Functional Reporting
LifeSphere LitPro builds a central repository for weekly hits to generate customized reports. Companies can also produce a report of marked activities.
Duplicate Check
LifeSphere LitPro performs duplicate checks of abstracts to identify unique and new relevant abstracts for each search. The duplicate check process includes/excludes ICSRs identified via the EMA medical literature monitoring process
Automatic Review of Abstracts and Full-Text Article Request
The solution can be automated to review abstracts for valid ICSRs and then issue a request for full-text articles. It can then route abstracts of full-text articles with valid ICSRs to the safety database.
Out-of-the-Box Readiness
The only proven and validated off-the-shelf solution to offer one platform for all safety surveilance needs, resulting in a more efficient drug development process and cost reductions.
Compliance Made Easy
Fulfills regulatory requirements by automating literature surveillance, event identification, data extraction, and case creation. This automated process decreases manual intervention and frees up teams to focus on core tasks.
Best-in-Class Implementation Partner
ArisGlobal wants to help make your journey as effortless as possible – not just at the beginning, but over the long-term. A multitude of support and service options, including Managed Services, Professional Services,
and Lifeshere Training.