Pharmaceutical Licensing Services
Delivering end-to-end software verification to ensure reliability, data integrity, and regulatory compliance across all development phases.
Why Choose Techvalio?
Our team combines industry expertise with advanced validation technologies. We create solutions that meet regulatory requirements and help your teams innovate confidently.
Our Approach: Agile, Scalable, Personalized
From assessment to delivery and support, we tailor the validation lifecycle to minimize risk and ensure compliance.
Key Benefits:
- Reduced audit deviations & documentation errors
- Faster validation lifecycle with agile methodology
- Regulatory alignment with FDA, EMA & WHO
What We Offer
Regulatory Consulting
Expert guidance on dossiers, process mapping, and globally recognized compliance documentation.
Validation & QA Services
Comprehensive risk analysis, protocol design, test execution, and ongoing system monitoring.
End-to-End Support
From GxP workshops to long-term support—with continuous improvement at every step.
Our Validation Process
Discovery
We analyze your systems, workflows, and compliance needs.
Gap Analysis
We identify missing validation and documentation requirements.
Testing & Documentation
Hands-on verification, test execution, and audit-ready documentation.
Launch & Support
Go live confidently with long-term compliance support.
FAQs
How long does a typical validation project take?
Most pharmaceutical validations take 6–12 weeks depending on system complexity.
Do you provide post-validation maintenance?
Yes, Techvalio offers periodic audits, documentation updates, and continuous compliance support.