Parivart™
parivart - change, a turning from one state to another · formerly Niyo360
Know which products a new rule touches, before the deadline finds you.
At a glance
- Category
- Regulatory Change Intelligence
- Theme
- Regulatory & Compliance
- Industries
- Healthcare, Manufacturing, Automotive, Retail & CPG
- Capabilities
- 6 composed
- Pairs with
- Tatvam, Drishti
Who it is for
- Regulatory affairs teams covering many markets
- Medical device and biopharma portfolio owners
- Automotive teams tracking hazardous material and environmental rules
Systems it sits on
EU MDR and FDA feeds · PLM systems · QMS · Regulatory information management systems
Also used in
Pairs with
Tatvam · Drishti
Explainer
Parivart in two minutes
A narrated walkthrough of the problem, how Parivart works, and what changes. Captions are available in the player.
Parivart is a regulatory change-intelligence platform. It continuously monitors global regulatory authority feeds and automatically maps new guidance against a company's active product-market portfolio. Instead of manually tracking bulletins, regulatory affairs specialists receive structured impact delta reports that highlight exactly which products, markets, and processes a new rule or amendment affects, cutting review time and reducing the risk of a missed compliance obligation.
The problem
Regulatory affairs teams track bulletins from dozens of authorities by hand, so the mapping from a new rule to the affected products and markets is slow, partial, and easy to miss.
The outcome
Structured impact reports that name exactly which products, markets, and processes a regulatory change affects.
How it works
How Parivart works
- 01
Monitor the authorities
Feeds from the relevant global regulators are watched continuously.
- 02
Read the change
New and amended guidance is parsed into the obligations it actually creates.
- 03
Map to the portfolio
Obligations are matched against the live product-market portfolio and the processes behind it.
- 04
Report the delta
A structured impact report names what is affected and routes it to the specialist who owns it.
Module 01
Authority Feed Monitoring
Global regulatory authority feeds watched continuously rather than checked periodically.
- 02
Portfolio Mapping
New guidance mapped against the active product-market portfolio it actually touches.
- 03
Impact Delta Reports
Structured reports naming affected products, markets, and processes, with the change highlighted.
- 04
Audit Readiness
A durable record of what changed, who assessed it, and what was done.
- rule to product, market, and process
- Mappedrule to product, market, and process
- monitoring across global authorities
- Continuousmonitoring across global authorities
Integrations
Ideal for
- Regulatory affairs teams covering many markets
- Medical device and biopharma portfolio owners
- Automotive teams tracking hazardous material and environmental rules
- Consumer goods teams following ingredient and formulation standards
Capabilities
Parivart composes these capabilities from the shared Agent Platform layer. The same atoms power the rest of the portfolio, so adopting a second accelerator reuses the integration work rather than repeating it.
Composition
Parivart is assembled from shared platform atoms. Hover a partner to see what you reuse on the next deployment.
- Document Intelligence
- Structure from unstructured sources: regulatory bulletins, specifications, contracts, claims, and reports.
- System Connectors
- MCP-connected reads and writes against the ERP, MES, PLM, CRM, and warehouse systems already in place.
- Risk Scoring
- Severity, likelihood, and exposure quantified consistently so prioritization survives an audit.
- Policy & Compliance
- Obligations from standards and regulations mapped onto live workflows and continuously monitored.
- Alert Routing
- Noise collapsed into the few signals that matter, routed to the person who can act with time to act.
- Evidence & Audit Trail
- Every input, decision, and action captured as tamper-evident evidence a regulator or auditor can follow.
Ingest
Ingest
Reason
Govern
Act
Govern
FAQ
Which authorities are covered?
Coverage is scoped to the markets you sell into. Medical device and biopharma feeds such as EU MDR and FDA are the common starting set.
Does it replace our RA specialists?
No. It removes the manual tracking and first-pass mapping so specialists spend their time on assessment and response.
How does it pair with Drishti?
Parivart watches the rules changing outside; Drishti evidences the controls inside. Together they close the loop between obligation and proof.