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 not only meet regulatory requirements, but also empower your teams to innovate with confidence.
Our Approach: Agile, Scalable, Personalized
From initial assessment to project delivery and ongoing support, we tailor our process to your business needs, minimizing risk and ensuring every system is compliant, resilient, and future-ready.
What We Offer
Regulatory Consulting
Expert guidance on submitting 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 initial GxP workshop to long-term maintenance—we’re with you at every step for continuous improvement.
Our Validation Process
Discovery
We learn your needs, systems, and compliance profile.
Gap Analysis
We identify what’s missing for full validation and compliant operation.
Testing & Documentation
Hands-on verification, robust documentation & digital records.
Launch & Support
Go live safely, then scale with confidence and continuous support.
“After switching to Techvalio’s pharmaceutical validation, our audit process became 2x faster and all documentation was instantly QC-ready.”
FAQs
How long does a typical validation project take?
Project timelines vary, but most pharmaceutical validations are completed within 6-12 weeks, depending on complexity.
Do you support post-validation maintenance?
Yes! We provide documentation updates, periodic audits, and compliance coaching as your systems and regulations evolve.