Opvia
Opvia, operating as Seal, is a London-based SaaS company that provides an AI-native GxP execution platform converting SOPs into controlled, validated workflows for pharmaceutical, biotech, and life sciences companies. Its AI agent neil and 48-hour onboarding differentiate it from legacy MES/QMS vendors.
- Company typePrivate
- Founded2019
- HeadquartersLondon, United Kingdom
- Headcount11–50
- GTM typeB2B
- OfferingSoftware
What Opvia does
Opvia Limited, operating commercially as Seal, is a London-based software company that builds an AI-native execution platform for GxP-regulated life sciences organizations. The platform ingests unstructured standard operating procedures (SOPs) — in PDF, Word, or paper-scan form — and converts them into controlled, executable digital workflows with review gates, e-signatures, operator training assignments, audit trails, and validation evidence. Its central AI agent, neil, is state-aware and proposes workflow builds from document clauses, surfaces deviations, compares run histories, and scopes process changes while the underlying system remains live. The product is delivered as a cloud-based SaaS suite comprising six blueprints — Manufacturing Execution System (MES), Quality Management System (QMS), QC LIMS, Tech Transfer, Electronic Lab Notebook (ELN), and Inventory Management — that share a common controlled execution spine.
Seal's technology is differentiated by the 48-hour build process, under which a single customer SOP is turned into a live, validated, controlled workflow with auto-generated validation evidence in two days — a step-change versus the multi-month revalidation cycles typical of legacy GxP stacks. The platform is designed for environments governed by FDA/EMA regulations and incorporates 21 CFR Part 11 compliance concepts, continuous audit trails, and change-control workflows that do not require taking processes offline.
Seal generates revenue through subscription SaaS contracts sold via a high-touch, consultative enterprise sales motion. Pricing is not publicly disclosed; prospects engage through "Talk to an Expert" and "Send us one SOP" calls-to-action, with the 48-hour build functioning simultaneously as a proof of concept and an onboarding mechanism. The company's target market is pharmaceutical, biotech, biologics, diagnostics, and adjacent GxP-adjacent companies — over 50 of which are referenced as customers, including Paradromics, Skye Biologics, Acclinate, Bioventix, MiAlgae, Agilent, Beckman Coulter, Ingenza, and Latitude Pharmaceuticals. Seal is venture-backed, having raised a seed round from Y Combinator and Cur8 Capital in 2020 and a follow-on round led by Liquid 2 Ventures in 2022, and is led by founder and CEO William Moss.
Opvia firmographics
Firmographics- Name
- Opvia
- Website
- https://opvia.io
- Company type
- Private
- Founded year
- 2019
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Opvia, operating as Seal, is a London-based SaaS company that provides an AI-native GxP execution platform converting SOPs into controlled, validated workflows for pharmaceutical, biotech, and life sciences companies. Its AI agent neil and 48-hour onboarding differentiate it from legacy MES/QMS vendors.
- Ownership category
- akta.pro rank
Opvia industry classification
Industry- Product category
- GxP Compliance Software
- NAICS
- Software Publishers (513210)
- SIC
- Services-Prepackaged Software (7372), Services-Computer Processing & Data Preparation (7374)
- akta.pro primary industry
- Computer System Validation (CSV) & GxP IT Compliance (21 CFR Part 11/Annex 11) (HLAGAKAG)
- akta.pro secondary industry
- OCR, ICR & Intelligent Document Processing (IDP) (BPAAAKAB)
Keywords
Where Opvia is headquartered
LocationHeadquarters
- HQ city
- London
- HQ country
- United Kingdom
- HQ region
- Europe
Markets served
Opvia business model
Business model- GTM type
- B2B
- Offering type
- Software
- Cost components
- Personnel, Technology or R&D, Marketing or Sales, Operations, Infrastructure
Revenue model
- SaaS Platform Subscription: Seal operates as a cloud-based SaaS platform for GxP-regulated companies, likely on a subscription basis. Pricing is not publicly disclosed and requires inquiry. The platform encompasses MES, QMS, LIMS, Tech Transfer, ELN, and Inventory modules under a unified controlled execution system.
Go-to-market motion1 record
Distribution channels1 record
Marketing channels3 records
Opvia product offering
Product offeringCore offering
Opvia operates "Seal," an AI-native GxP execution platform that converts SOPs, batch records, methods, and forms into controlled digital workflows with real-time evidence capture, e-signatures, review gates, training integration, and audit trails. The platform serves GxP-regulated pharmaceutical, biotech, biologics, and life sciences companies with modular blueprints for manufacturing execution, quality management, QC LIMS, tech transfer, electronic lab notebooks, and inventory management.
Product overview
Seal is an AI-native GxP execution platform that transforms static SOPs into controlled, executable workflows. The core platform uses an AI agent called neil to parse documents and generate workflows with compliance features. The platform offers a modular architecture with specialized blueprints including MES (Manufacturing Execution System), QMS (Quality Management System), QC LIMS, Tech Transfer, ELN (Electronic Lab Notebook), and Inventory Management modules. All modules share a common execution spine with integrated training, approvals, audit trails, and validation evidence.
Differentiator
Problem solved
Functional benefit
Products and services
- Seal AI-native GxP execution platform that transforms SOPs, batch records, methods, and forms into controlled digital workflows with real-time evidence capture, e-signatures, review gates, training integration, and audit trails. First process goes live within 48 hours. Built for GxP-regulated life sciences companies including pharmaceutical, biotech, biologics, and medical device organizations. Modular blueprints cover MES, QMS, QC LIMS, Tech Transfer, ELN, and Inventory Management.
- neil State-aware AI execution agent within the Seal platform that reads SOPs (PDF, Word, or paper scans), proposes workflow builds, scopes changes, identifies missing checks, compares run history, simulates next changes, and routes approvals through the controlled system.
Quantifiable outcome
- 90% less time on traveler review
- +5 more outcomes
Companies that use Opvia
Customer profileNamed customers9 records
Segments1 record
Ideal customer profiles1 record
Opvia technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
AI capability4 records
Feature4 records
Opvia partnerships and signals
Strategic signalScale indicators5 records
Recent moves6 records
Expansion highlights5 records
Opvia competitors and assessment
Company assessmentBroad incumbents
- Veeva Systems: Dominant life sciences cloud platform with Veeva Vault covering quality, regulatory, and clinical documents. Directly competes with Seal in the GxP/QMS layer but serves a much broader portfolio across pharma.
- LabWare: Established LIMS and laboratory informatics vendor used across pharma, biotech, and applied markets. Directly competes with Seal's QC LIMS blueprint and shares GxP validation requirements.
Direct peers
- MasterControl: Long-standing GxP quality and manufacturing execution platform used by pharma/biotech/medical device companies. Directly competes with Seal's QMS and MES modules for the same regulated customer base.
- Dot Compliance: AI-enabled QMS and quality management for life sciences on Salesforce. Competes with Seal in digitizing SOPs and quality workflows under GxP, with a similar focus on modern UX and faster deployment.
- Kneat (Smart Pharma): Electronic validation and process execution software purpose-built for GxP-regulated life sciences. Directly comparable to Seal's validation evidence generation and controlled workflow capabilities.
- Qualio: Cloud QMS designed for life sciences startups and mid-market pharma/biotech. Competes with Seal's QMS blueprint for the same early-to-mid-stage GxP customer segment.
Emerging players
- Greenlight Guru: QMS platform purpose-built for medical device companies under FDA/ISO 13485. Comparable to Seal in modern UX and vertical specialization, but narrower scope (medical devices only).
- QT9 Software: Cloud QMS with life sciences and manufacturing modules. Competes for the same mid-market GxP customer base as Seal, though with a more traditional QMS-only positioning.
- SimplerQMS: Cloud QMS designed for pharma, biotech, and medical device companies under GxP and 21 CFR Part 11. Directly comparable to Seal's QMS module with a similar compliance-led value proposition.
- Tulip: Frontline operations and manufacturing execution platform increasingly adopted in life sciences. Comparable to Seal's MES blueprint and shared emphasis on connected operator workflows and real-time data capture.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat5 records
Key risks6 records
Key highlights7 records
Customer concentration
Opvia social profiles
Digital presenceOpvia financial estimates
Financial estimateRevenue estimate
Valuation estimate
Opvia leadership team
Management profileNumber of profiles
Profiles1 record
Opvia funding detail
Funding detailFunding overview
Funding rounds2 records
Investors3 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Opvia M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Opvia
What does Opvia do?
Opvia operates "Seal," an AI-native GxP execution platform that converts SOPs, batch records, methods, and forms into controlled digital workflows with real-time evidence capture, e-signatures, review gates, training integration, and audit trails. The platform serves GxP-regulated pharmaceutical, biotech, biologics, and life sciences companies with modular blueprints for manufacturing execution, quality management, QC LIMS, tech transfer, electronic lab notebooks, and inventory management.
When was Opvia founded?
Opvia was founded in 2019. It employs 11 to 50 people.
Where is Opvia based?
Opvia is headquartered in London, United Kingdom, in the Europe region.
How does Opvia make money?
One revenue line is on record: saaS Platform Subscription.
Who are Opvia's main competitors?
Broad incumbents on record are Veeva Systems and LabWare. Direct peers are MasterControl, Dot Compliance, Kneat (Smart Pharma) and Qualio. Emerging players are Greenlight Guru, QT9 Software, SimplerQMS and Tulip.
Does Opvia have an API?
No public API is recorded for Opvia.
What industry is Opvia in?
Opvia's product category is GxP Compliance Software. Its primary akta.pro industry code is HLAGAKAG, Computer System Validation (CSV) & GxP IT Compliance (21 CFR Part 11/Annex 11), with a secondary code of BPAAAKAB, OCR, ICR & Intelligent Document Processing (IDP). Its NAICS code is 513210 and its SIC code is 7372.