Provaxa
Translating medicine for a better life
Full spectrum clinical solutions from concept to cure, Clinical Studies, Advanced Therapies, and Life-Saving Biologics
Your Strategic and Trusted Medical Research Partner
We bring together a single window and powerful network of services offering integrated solutions for sponsors seeking speed, compliance, and innovation in global markets. With a shared commitment to ICH-GCP, ISO-certified quality systems, and related regulatory excellence, we accelerate pathways from concept to cure.
Provaxa follows a multi-faceted approach, encompassing advanced technologies, optimized clinical studies, and improved collaboration between researchers and industry. This involves streamlining clinical study processes and fostering stronger partnerships to translate research into tangible patient benefits.
Our Services
Comprehensive solutions across all phases of clinical development and advanced therapies
Preclinical Studies
Accelerating Discovery. Advancing Therapies.
In vitro & in vivo studies, pharmacokinetics, toxicology testing, drug formulation, and GLP-compliant regulatory support.
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Clinical Studies
Driving Research, Delivering Results
Feasibility, regulatory submissions, monitoring, data management, biostatistics, and quality oversight across all therapeutic areas and phases.
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Stem Cell & Gene Therapy
Powering Life Through Genetic Innovation
ATMP clinical study design, GMP-compliant processing, patient recruitment, long-term follow-up, and global regulatory alignment.
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Biopharmaceuticals
From research to real-world care, delivering WHO-prequalified vaccines and therapies that save lives
R&D and process development, GMP manufacturing, stability studies, quality control, technology transfer, and WHO prequalification.
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Pharmacovigilance
Guarding Health Through Vigilance
AE/SAE reporting, signal detection, risk management, safety database management, PSUR/RMP preparation, and regulatory compliance.
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Medical Affairs
Driving Clinical Excellence Through Medical Expertise
Scientific liaison, evidence-based medical communication, KOL engagement, real-world evidence, post-marketing surveillance support.
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Unique advantages that set us apart as your strategic research partner
One Partner, One Solution
Comprehensive end-to-end services covering the entire drug development lifecycle, no need to juggle multiple vendors.
Global Presence & Expertise
Strong footprint across India, Africa, Europe, and UAE with deep regulatory knowledge of CDSCO, EMA, US FDA pathways.
Proven Track Record
Extensive experience backed by a global portfolio of successful sponsors spanning preclinical research to post-marketing surveillance.
Regulatory Excellence
ISO-certified quality systems, ICH-GCP compliance, and proven expertise navigating complex global regulatory environments.
Full-Spectrum Clinical Solutions
From end-to-end clinical studies to Stem Cell & Gene Therapy to life-saving biologics, we cover the full drug development continuum with integrated excellence.
Let's Accelerate Your Next Breakthrough
From protocol to product launch, partner with us for speed, compliance, and innovation in clinical research.