VOXTURCLINICAL RESEARCH
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Phase I–IV clinical trials and BA/BE studies across India, backed by more than 20 years of scientific and operational experience.
Study design, feasibility and regulatory strategy are built into the protocol from the first draft, so the study is shaped for its submission from day one.
A network across India for patient recruitment and site coordination, matched to each study’s population and phase.
Trial management and GCP-compliant site monitoring keep data clean, so the reports that follow stand up to scrutiny.
Regulatory consulting carries molecules from the Indian clinic to regulated markets, including the questions that come after submission.
Four integrated service lines covering the full study lifecycle, from protocol design to regulatory submission.
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Full-lifecycle management of Phase I to IV trials, from protocol design and feasibility to conduct, close-out and the final study report.
02Risk-based onsite and remote monitoring, source data verification and safety oversight that protect data integrity.
03Statistical design, analysis and reporting: sample size, SAP, ISS/ISE, interim analysis and DSMB support.
04GxP audits, compliance assessment and submission support for USFDA, EMA, TGA and other regulatory filings.
Studies executed for USFDA, EU and TGA review, alongside dermatological, biomarker and nutraceutical programmes.
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Bioanalytical, project management and quality assurance experience, in the same room as your study.
Founder of Voxtur Clinical Research, with a BTech in Chemical Engineering from Anna University. Previously with KMS Health Center, Luminol Biopharma and Micro Therapeutic Research Labs. Runs studies to TGA, USFDA and EMA guidelines.
MBA from Madras University. Leads project management for oncology trials, from site management through final reporting, with close adherence to industry standards.
M.Sc. in Analytical & Biopharmaceutical Technology from Anna University. Oversees quality systems for bioanalytical method validation, clinical sample processing and analytical data review.
Voxtur Clinical Research supports pharmaceutical and biopharmaceutical companies with clinical trials and BA/BE studies across India, from study planning through execution and site coordination.
Our experience includes complex clinical studies, with a growing focus on oncology and other specialised research areas.
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Voxtur Clinical Research is a clinical research company (CRO) in Chennai, India. We run clinical trials and Bioavailability / Bioequivalence (BA/BE) studies for pharmaceutical and biopharmaceutical companies. The work covers protocol design, regulatory and ethics approvals, site tie-up, patient recruitment, monitoring, data management, statistical analysis and the signed clinical study report.
Yes. Our project management team has overseen 750+ BA/BE studies. We run BA/BE studies for regulated and non-regulated markets, with bioanalytical quality systems built for USFDA, ANVISA and MoH review.
Send us the product, the indication and what the data is for. We reply with a quotation, with optional biomarkers quoted separately. Once you confirm it with a work order, we start preparing the protocol.
Every study in India runs under CDSCO / DCGI approval and ethics committee review, in line with the New Drugs and Clinical Trials Rules 2019. For sponsors filing in regulated markets, we conduct studies to ICH-GCP and prepare data and documentation for USFDA, EU and TGA review.
We match the indication to sites from our network of 75+ hospitals and site management organisations, each with a registered ethics committee, and 125+ registered investigators. We run site feasibility and investigator selection first, and the feasibility results come to you with the recommendation.