INDUSTRY MEMBERSHIP
CDISC member
Synovah HealthTech is a member of the Clinical Data Interchange Standards Consortium.
Explore the CDISC member communityAI FOR LIFE SCIENCES
Life sciences,
intelligently
connected.
Bring clarity to complex workflows. Purpose-built AI for patient safety, clinical intelligence, and the data that connects them.
Built around science.Designed for people.
SYNOVAH / CONNECTED INTELLIGENCE01
From information
to possibility.Science meets
intelligent technology
to possibility.Science meets
intelligent technology
For the people
moving life sciences forward
PharmaceuticalsBiotechnologyCROsClinical research
MEMBERSHIP & RECOGNITION
Part of the community moving life sciences forward.
ENTREPRENEURSHIP RECOGNITION
Selected for the Zonal round
Synovah HealthTech was selected for the Eureka! 2026 Zonal round, organized by E-Cell, IIT Bombay.
About Eureka! at IIT Bombay01 / OUR PRODUCT ECOSYSTEM
Specialist tools.
Shared ambition.
Explore the right starting point for your team—from safety intake to clinical data insight. Watch a short feature explainer for each product.
PHARMACOVIGILANCE01
SynoPVLM
End-to-end Pharmacovigilance Automation
AI-assisted case intake, triage, signal detection, and regulatory reporting.
Safety operations
ADVERSE EVENT INTAKE02
SynoSafetyBOT
Intelligent Adverse Event Reporting Chatbot
Conversational adverse event reporting with structured capture across web, mobile, and voice.
Patient & HCP engagement
DATA EXTRACTION03
SynoMINER
Comprehensive Data Extraction & Analysis
Extract and analyze information from PDFs, emails, databases, and clinical documents.
Information discovery
METADATA MANAGEMENT04
SynoSYS
Centralized Metadata Management Platform
Centralized metadata, version control, audit trails, and CDISC compliance.
Study data standards
REPORTING & ANALYTICS05
SynoPRO
Advanced Reporting & Visualization
Interactive dashboards, customizable reporting, and real-time data visualization.
Decision support
02 / FROM COMPLEXITY TO CLARITY
Start with the work.
Make it flow.
Every team has a different bottleneck. Start where information gets lost, effort gets repeated, or insight arrives too late.
WORKFLOW FOCUS01 / 03
Make the first interaction count.
Help information enter the workflow in a form your team can work with.
01
Reporter conversations
02
Case intake and triage
03
Documents and source data
03 / OUR DESIGN PRINCIPLES
Intelligent technology.
Human purpose.
In life sciences, technology earns its place by making real work clearer, more consistent, and easier to manage.
People at the centre
Build around the people who report, review, and act on information. Keep the needs of patients and practitioners in view.
Quality as a starting point
Consider data quality, traceability, and review needs from the beginning of the workflow.
Science with a practical lens
Use AI to address a defined problem. Align the solution with the team, the information, and the decisions it supports.
04 / ABOUT SYNOVAH
Where synergy
meets innovation.
We believe the next chapter of life sciences will be shaped by how well people, information, and intelligent technology work together.
Synovah HealthTech develops AI-powered solutions across pharmacovigilance, clinical research, and data management. Our focus is practical: help teams turn complex information into more useful workflows.
From India, with a global ambition—to make life sciences work better for the people it serves.
Build the next chapter with us05 / A FEW USEFUL ANSWERS
Let’s make
it clear.
Which product should we start with?
Start with the workflow you want to improve. SynoPVLM and SynoSafetyBOT address safety operations and reporting. SynoMINER, SynoSYS, and SynoPRO focus on data and insights. We can help map your needs in a discovery conversation.
Can we explore a single solution?
Yes. A demo can focus on one product and a specific workflow. Share the information you work with, the systems involved, and what your team wants to improve.
What about regulatory and validation requirements?
Requirements vary by product, intended use, and deployment. During discovery, discuss your applicable standards, validation expectations, security needs, and review controls. Request the relevant evidence before making a qualification decision.
What should we include in a demo enquiry?
Tell us your role, company, product of interest, and the workflow you want to explore. Please keep your initial enquiry free of patient information and confidential records.
06 / LET’S BUILD WHAT’S NEXT
Your next step
starts with a
conversation.
Bring us a workflow, a challenge, or an idea.
Let’s explore where intelligence can make a difference.
Explore a solution
Choose your area of interest to prepare a demo enquiry.
Prepare demo emailOpens an editable draft in your email app.
BASED IN INDIABuilt for life sciences, everywhere.