RightOrigins will be attending CPHI Milan at Fiera Milano from 6–8 October 2026.
-Compliance questionnaires.
-Audit evidence.
-PPWR requirements and packaging data.
-Supplier documents and product specifications.
-ESG data requests.
If completing these tasks means searching across systems, chasing colleagues and rebuilding answers that already exist somewhere, let’s talk at CPHI Milan.
Our purpose-built AI agents automate the repetitive work behind compliance. From collecting supplier information and answering compliance questionnaires to validating Certificates of Analysis and preparing audit-ready information, show us your most time-consuming task, and we’ll show you how to automate it.
The goal is to give quality and compliance teams more time to assess risk, make decisions and protect the business.
Bring us a practical compliance challenge
Our meeting at CPHI will be a practical conversation about the hidden administrative tasks that create unnecessary work for quality and compliance professionals, and how to tackle them with AI. You could bring us a challenge involving:
Questionnaire or RFI response
CoA verification
Supplier qualification
Product specification alignment
Supplier certification management
Missing or inconsistent compliance information
Product and batch traceability
Audit preparation
Bring us your day-to-day challenge. Together, we’ll map how your supply-chain compliance process works, identify where the bottlenecks sit and explore what a better approach could look like.
There is no need to share confidential information. Simply tell us which workflow you would most like to improve.
What can RightOrigins automate?
RightOrigins can help remove administrative work from multiple areas of your compliance operations.
Questionnaire/RFI response: Purpose-built AI agents automate regulatory, sustainability, or customer questionnaires and information request, reducing the turn around time by 80%.
Compliance validation: It can also conduct field-level, cross-field and cross-document validation to identify inconsistencies, missing information and potential deviations.
CoA verification: it can extract key values from Certificates of Analysis and compare them with approved product specifications and internal inspection plans.
PPWR and packaging compliance: RightOrigins can help teams collect and structure packaging data, connect supplier evidence to applicable PPWR requirements, identify missing information and support the preparation of technical documentation and declarations of conformity.
Completeness checks: RightOrigins AI can perform completeness checks to verify that required documents, fields and supporting information are present before a product, supplier or batch moves forward.
Supplier data collection: Our AI agents can collect required information, identify missing submissions and reduce repetitive follow-up across your supplier network.
Certification management: The platform can extract and structure supplier certification data, connect it to the relevant products and suppliers, and improve visibility of compliance status.
Product compliance data: It can also transform fragmented product and supplier information into standardised, validated records that support ERP, PIM and operational workflows.
Traceability: By connecting compliance evidence to the correct supplier, material, product and batch, RightOrigins strengthens traceability and helps you understand where information came from and what it supports.
Audit and regulatory preparation: It enables you to retrieve validated data and supporting evidence more efficiently when an auditor, customer or regulatory stakeholder requests information.
Who should meet RightOrigins at CPHI?
The conversation is designed for professionals working across:
Quality and quality assurance
Regulatory affairs and compliance
Supply chain and procurement
Technical and commercial operations
Product information and specifications
Sustainability and ESG
Digital transformation
Whether you work for a pharmaceutical manufacturer, CDMO, API producer or ingredient supplier, bring the process your team knows takes too long.
What you’ll walk away with?
In 30 minutes, you’ll receive a practical implementation guide for applying AI within your quality and compliance workflows, grounded in your current challenges and priorities.
Why should you meet us?
The conversation will be grounded in what has already worked in real compliance environments. For one European ingredient manufacturer, RightOrigins reduced RFI turnaround time by 80% within three months while creating a central source of approved compliance and sustainability information.
The value was not simply faster answers. Teams spent less time searching for evidence, repeating work and coordinating inputs across departments.
At CPHI, we will use the same outcome-led approach to assess your challenge. Rather than beginning with the technology, we will look at the volume of manual work, the people involved, the information sources being checked and the controls that must remain with your experts.
This helps determine whether AI can deliver a meaningful result and which measures should define success, from shorter cycle times and fewer supplier follow-ups to improved data completeness, traceability and audit readiness. You will leave with a practical starting point for your organisation, not a generic AI pitch.
Spend more time strengthening compliance
Meet RightOrigins at CPHI Milan and discover how purpose-built AI agents can remove repetitive work from your compliance workflows while keeping your experts in control.
Book a meeting with RightOrigins at CPHI Milan.