What is Low-Code Studio in Veritas GxP?
Low-Code Studio is a visual process configuration capability within the Veritas GxP platform that lets pharmaceutical manufacturers design and customize eBMR workflows using drag-and-drop components, without traditional programming for every process change.
It provides a configurable layer between your manufacturing process and Veritas GxP modules, letting you define how different capabilities participate in a specific batch workflow — configured in weeks instead of the 6–9 months a custom-coded workflow change typically takes, while staying aligned to US FDA and India CDSCO requirements.
Why Pharmaceutical Processes Need Flexible Configuration
Every pharmaceutical manufacturer has different manufacturing sequences, approval requirements, quality checks, material activities, equipment interactions, and operational responsibilities. A fixed workflow forces the organization to change its process to fit the software — and traditional development to accommodate that difference can take 6–9 months per change.
Low-Code Studio takes the opposite approach: configure the software around your process, visually, in weeks. Organizations define their process and determine which Veritas GxP capabilities are required at each stage, without opening a development backlog.
Common Challenges in Pharmaceutical Manufacturing
Low Code Studio Designed for Pharmaceutical Manufacturing
Visual Workflow Designer
Design manufacturing workflows through an intuitive drag-and-drop interface instead of custom-coding every interaction.
Drag-and-Drop Process Configuration
Add, arrange, and configure workflow components according to the required manufacturing sequence.
Modular Process Design
Select relevant Veritas GxP capabilities and organize them into the required manufacturing workflow.
eBMR Workflow Configuration
Configure how manufacturing activities are executed and recorded within the Electronic Batch Manufacturing Record.
Process Sequencing
Define the order in which manufacturing activities, checks, approvals, and related actions occur.
Conditional Workflows
Configure process paths based on defined business conditions, process requirements, or workflow rules.
Configurable Approvals
Define where review and approval activities are required within the manufacturing process.
Quality Integration
Include quality checks, inspections, deviations, and other quality activities at appropriate workflow stages.
Material & Equipment Integration
Connect material- and equipment-related activities directly into the configured manufacturing workflow.
Role-Based Activities
Assign workflow activities according to configured user roles and responsibilities.
Rapid Configuration Architecture
Deploy new or modified workflows in weeks, replacing the 6–9 month cycle traditional development requires.
Dual Regulatory Configuration
Build workflows with approvals, signatures, and audit trails aligned to both US FDA 21 CFR Part 11 and India CDSCO.
Workflow: From Process Design to Controlled Batch Execution
Define Process
Identify the manufacturing sequence, activities, decisions, approvals, and controls required for the process.
Select Components
Choose the relevant Veritas GxP capabilities required within the manufacturing workflow.
Drag & Drop
Visually arrange workflow components into the required process sequence.
Configure Activities
Define activities, responsibilities, data requirements, and process-specific parameters.
Define Rules
Configure supported conditions and workflow logic that determine how the process progresses.
Configure Approvals
Add required review and approval points based on organizational responsibilities.
Validate Workflow
Review and verify the configured process before making it available for controlled execution.
Release Configuration
Release the approved workflow configuration for use within the appropriate manufacturing process.
Execute Through eBMR
Execute the configured manufacturing process through the Electronic Batch Manufacturing Record.
Track & Improve
Use traceability and operational insights to identify opportunities for process improvement.
Benefits: Build Manufacturing Workflows Around Your Business
Greater Process Flexibility
Configure supported manufacturing processes according to operational requirements, not software limitations.
Faster Configuration
Deploy new or modified workflows in weeks, cutting configuration time by [X]% versus traditional development.
Reduced Development Effort
Configure workflows through reusable components rather than building every process interaction from scratch.
Better Operational Alignment
Make the software workflow reflect how manufacturing teams actually work.
Consistent Execution
Standardize approved workflows while retaining controlled process flexibility.
Easier Process Evolution
Adapt configured workflows in weeks as products, processes, or operational requirements change.
Connected Manufacturing
Bring relevant Veritas GxP capabilities together within a unified, configurable process.
Improved Traceability
Maintain controlled workflow history, activities, approvals, and execution records.
Deploy Faster Than Traditional Development
Go live in weeks instead of the 6–9 months custom-coded workflow changes typically require.
Stay Aligned Across Two Regulators
Configure approvals, signatures, and audit trails that satisfy both US FDA 21 CFR Part 11 and India CDSCO.
Compliance: Configurable Processes with Controlled GxP Execution
GMP
Support controlled manufacturing workflows and standardized process execution.
US FDA 21 CFR Part 11
Support electronic records, electronic signatures, access controls, and audit trails within regulated workflows.
India CDSCO
Configure workflows, approvals, and audit trails aligned with India's CDSCO regulatory expectations.
EU GMP Annex 11
Support controlled configuration and computerized-system processes within pharmaceutical operations.
ALCOA+
Maintain attributable and traceable data throughout configured manufacturing workflows.
Audit Trail
Track relevant configuration changes and regulated workflow activities.
Electronic Signatures
Support authenticated approvals at configured workflow stages where required.
Role-Based Access
Control who can configure, approve, and execute applicable workflows.
Why Veritas GxP for Low-Code Configuration
Veritas GxP Low-Code Studio gives pharmaceutical manufacturers the flexibility to configure manufacturing processes without turning every process change into a traditional software-development project.
Its visual drag-and-drop approach lets organizations bring relevant Veritas GxP capabilities together and define how they participate in an eBMR workflow, so the platform adapts to the process — not the other way around.
Configuration speed is the differentiator here. Where a traditional development cycle takes 6–9 months to implement a single workflow change, Low-Code Studio compresses that to weeks, letting manufacturing and quality teams respond to new products, sites, or regulatory changes without a development backlog.
Veritas GxP is also built for manufacturers configuring processes across two regulatory regimes. Approvals, electronic signatures, and audit trail requirements for both US FDA 21 CFR Part 11 and India CDSCO are available as configurable components, so a single workflow can satisfy both regulators without parallel builds.
Because Low-Code Studio configures workflows using the same connected Veritas GxP capabilities as eBMR, Quality Management, Material Management, and Equipment Management, every workflow it produces inherits controlled execution, approvals, traceability, and data integrity by default — configuration flexibility never comes at the cost of compliance.
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+91 9260246321Low-Code Studio is a visual configuration capability that lets organizations design and customize supported manufacturing workflows using configurable components rather than traditional programming for every change.
No. Low-Code Studio is a platform capability within Veritas GxP that lets customers configure manufacturing workflows and connect relevant Veritas GxP capabilities — it isn't sold or deployed separately from the platform.
Workflow configuration and release typically takes weeks, compared to the 6–9 months a traditional custom-coded workflow change requires.
Yes. Workflows can be configured with approvals, electronic signatures, and audit trails aligned to both US FDA 21 CFR Part 11 and India CDSCO.
Yes. Low-Code Studio is designed to let customers configure supported eBMR process flows according to their manufacturing requirements.
The objective is to minimize traditional development for supported workflow configuration by providing visual, drag-and-drop configuration capabilities.
Yes. Workflows can be configured according to applicable product, process, operational, quality, and approval requirements.
Yes. Configurable approval activities can be incorporated at appropriate stages of the manufacturing workflow.