Regulatory and Clinical Staffing Services in Thailand







- Inhouse team of regulatory and clinical professionals with 5 – 25 years of experience
- Deep domain expertise to understand staffing requirements and find suitable candidates
- Experience across complex and diverse therapy areas
- Diverse products experience – Pharmaceuticals, Medical Devices, Biologics, Radiopharmaceuticals, and Combination Drugs
- Network of regional, experienced professionals available on short notice
- Fast, efficient, and client-centric solutions for all staffing needs
- Hourly and monthly flexible engagement models with tenures starting from 3 months
- New Product Registration (New Chemical Entities, Generics, Biologics, Biosimilars, Radiopharmaceuticals, Medical Devices – all classes, IVD, Combination Drugs)
- Lifecycle Maintenance – Variations, Renewals, Withdrawals, Artwork Review
- Regulatory Intelligence, Monitoring, and Strategy
- Thai FDA Liaison, Response to Queries
- Distributor Coordination and Training
- Advertisement and Promotional (Ad Promo) Material Review
- Regulatory Information Management, Database Update, and Maintenance
- Thai FDA Meetings and Strategy
- Tenure: 3, 6 and 12 months or longer
- Models: Hourly, Monthly engagement billed monthly
- 5 – 25+ years
- Strategic to operational role experience
- New registrations to lifecycle maintenance work experience
- Clinical Trial Monitoring and Management
- Clinical Data Management
- Site Management and Patient Engagement
- Clinical Data Science, Real World Evidence Analysis
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 ?
Specialized Regulatory
Services Across Multiple Industries
Expert Regulatory Services To Streamline Compliance

Regulatory Intelligence & Strategy

Medical & Technical Writing

Publishing & Submission






Regulatory Services Across Multiple Countries

India

Singapore

Mexico

Brazil

Vietnam

Malaysia

Argentina

Colombia

Taiwan

China

European

Thailand

Indonesia

Philippines

USA

Japan

Qatar

South Korea
Tips & Articles

Prioritizing Genes from Publicly
Artixio has developed an artificial intelligence based solution generating a list of prioritized genes...

CDSCO Simplifies Subsequent Importer
India’s regulatory authority, the Central Drugs Standard Control Organization (CDSCO), has published an important...

AI For Monitoring Regulatory
Regulations in pharma and medical devices don’t stand still. They change as new technologies...