Regulatory AI Consulting Services
AI Solutions for Pharma, MedTech, and Life Sciences — Practical consulting and development services focused on regulatory intelligence, compliance, and process efficiency.
AI-Driven Compliance Services by Artixio
Artixio’s team includes professionals who have been pioneers in developing cutting edge AI solutions enabling faster time to market for pharmaceutical and medical devices across the product lifecycle and value chain. Right from drug development to regulatory affairs and ongoing regulatory intelligence, Artixio offers off the shelf AI based tools coupled with strategic digital transformation consulting and custom application development services for the life sciences industry leveraging machine learning, predictive analytics, deep learning and NLP.
We Help Lifesciences Industry Realize Full Potential of AI through Integration and Custom Development:
Our Regulatory AI Services
Leverage Artixio’s AI experience to achieve your AI transformation goals. From discovery to planning and implementation, we ensure responsible AI practices and data governance in compliance with regulations and ethics.
Transform your ideas and concepts into frugal proof of concept and pilot tools to validate your plans. We offer express prototyping to help you visualize your ideas, define user functionalities, user validation and enhancements to ensure faster time to market for your ideas.
Our fast-paced AI web and mobile app development solutions can help your innovations to bring to live quickly, efficiently and securely. We build AI powered apps supporting entire drug development and regulatory value chain working in collaboration with you.
Integrate AI within your existing systems seamlessly using our custom integration consulting and services to transform your current systems and maximize efficiency with minimum disruption and business continuity.
Right from Data Analysis, Regulatory Intelligence, Document Authoring and Workflow Automation, leverage our custom GenAI solutions to maximize AI’s potential in your R&D, Clinical and Regulatory business. Our transformative solutions leverage models such as GPT, Llama, PaLM, Mistral and others.
Drive strategic decisions harnessing your enterprise data by leveraging our data analytics capabilities to dive deep in to your datasets across R&D, Clinical, Regulatory and Supply Chain.
Pharma & Medical Devices organizations have huge legacy data archived in silos across departments. To fully realize the power of AI and generate answers to key business situations, it is imperative to structure, annotate and transform data into meaningful datasets. Further, managing such data requires alignment with AI transformation objectives but most importantly, a deep subject matter expertise across Clinical, Regulatory Affairs and Drug Development. Artixio is uniquely positioned as a partner with best of both worlds backed by decades of proven experience in deploying regulatory teams for seamless data management enabling digital transformation.
- Regulatory, Clinical Domain Experts
- Data Scientists
- AI/ML Engineers
- Software Architects
- AI Product Managers
- Compliance & Validation Experts
Solutions We Have Built:
Global Drug Portfolio Intelligence Platform (QuriousPI)
- Disease Portfolio Analysis
- Disease Area Insights
- Pipeline Analysis
- Scenario Planning
- Portfolio Benchmarking
Functions Supported:
- Portfolio Management
- Regulatory Intelligence
- Dossier Compilation
- Labeling Authoring and Review
- Artwork Review and Update
- Competitor Analysis
- Distributor Intelligence
- Data Pipeline
Global Regulatory Intelligence Platform (QuriousRI)
- Global Predicate Analysis for Drugs and Devices
- Regulatory Classification Assessment
- Regulatory Pathway Analysis
- Regulatory Guidelines and Insights
- Compare Regulations
- Dossier Requirements
- Dossier Gap Analysis
- Assisted Document Authoring
- Global Submissions Management
- Ongoing Regulatory Intelligence Monitoring & Impact Analysis
- Competitor Tracking and Intelligence
Why Artixio For Your AI Regulatory Services?
- Deployed AI Solutions for Global Top 10 Pharma and MedTech/BioTech/HealthTech Startups
- Proven Experience Across Drug/Device Development, Regulatory and Clinical Processes
- Regulatory, Clinical Domain Experts and AI Architects for Solution Design
- Data Governance, System Validation and Audit Trail Management
- Full-Stack Engineers for Secure and Scalable Development
- Efficient Product and Project Management
- Regulatory/Clinical Experts for Data Management, Annotation and Ongoing Maintenance
FAQs
What type of companies does Artixio support with AI Consulting, Solutions and Development Services?
Artixio supports large pharma and medtech companies, AI first medtech/biotech and healthtech startups, Regulatory and Pharmacovigilance consulting services providers, Clinical Research Organizations, CDMOs and others.
How is Artixio different from traditional IT consulting companies?
Artixio brings unique combination of Regulatory, Development, Clinical and PV expertise coupled with Data Sciences and AI engineering. Our solutions are deeply rooted in our regulatory, development and clinical experience across functions within pharma and medtech companies as well as real-time challenges faced by companies solving practical problems.
Can Artixio help setup an Internal AI Center of Excellence?
Yes, Artixio can help define the vision, organization structure, team composition, operating model and roadmap for AI center of excellence within client organization. Artixio also helps setup the COE in global model with teams located in multiple low cost locations.
Does Artixio provide off-the-shelf SaaS solutions or On Site deployment?
Artixio offers both web based applications as well as solutions deployed onsite within client company’s IT environment as per their secure IT policies.
Does Artixio provide custom AI tools development?
Yes, right from custom point solutions for specific function or workflow automation to enterprise level AI solutions, Artixio offers end to end solutions.
Still Have Questions ?
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Expert Regulatory Services To Streamline Compliance
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Regulatory Services Across Multiple Countries
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