Batch record review agent
Checks batch records against the master recipe and specification, and highlights exceptions only.
Human approval before any system of record changes
Manufacturing · Process Manufacturing
Recipes, specifications and batches on one thread.
From formulation to plant, we connect recipe, specification and quality data with ERP so every batch is made to the current, approved specification.
Industry challenges
What holds Process Manufacturing operations back.
Challenge 01
Recipes in spreadsheets
Formulations and specifications live in files that are hard to version and harder to audit.
Challenge 02
Batch genealogy gaps
Tracing a batch back to raw material lots and specifications takes far longer than it should.
Challenge 03
Plant-to-ERP disconnect
Quality and production data from the plant rarely flows cleanly back into ERP.
How we help
Four practices, applied to how your industry really works.
Engage one practice or the full journey. The same team carries the work from diagnosis to agents in production.
- 01 · DiagnoseStrategy
Operations & Data Diagnostics
Assess specification management and batch traceability maturity.
Explore the practice - 02 · ArchitectRoadmap
Technology Landscape & Process Engineering
Design the recipe-to-plant landscape across PLM, MES, LIMS and ERP.
Explore the practice - 03 · ImplementDelivery
PLM & ERP Implementation
Prabandh or enterprise PLM for recipes and specifications, integrated with plant systems.
Explore the practice - 04 · AutomateAgentic AI
AI Agents & Process Automation
Agents that review batch records and triage quality deviations.
Explore the practice
Industry brief · Prabandh
Download PDF Process Manufacturing industry brief
For food, chemicals, Ayurveda, cosmetics and other batch manufacturers: one thread from formula to ledger. Two pages, from prabandh.in, the PLM + ERP platform we deliver as a channel partner.
AI agents
Agents built for Process Manufacturing work.
Examples of the agents we design for this industry. Each one works inside your systems and hands decisions to a named person for approval.
Quality deviation agent
Triages deviations, links them to batch, lot and supplier, and drafts the CAPA for review.
Human approval before any system of record changes
More industries
From under the sea to the sky.
Life sciences
Pharma
Formulation, specification and change control with GxP traceability.
Life sciencesLife Sciences
Design history, validated change control and regulatory submissions.
HealthcareHealthcare
Supply, asset and inventory flows across providers, with traceability built in.
WellnessAyurvedic Wellness
Classical formulations, herb sourcing, batch records and AYUSH compliance.
Start a conversation
Talk to a partner who knows Process Manufacturing.
Share where your operations are stuck and a partner will come back with a working view of what to do first. No sales script.