Empowering Clinical Research Excellence
At Vidhur Life Sciences, we specialize in comprehensive Clinical Research consultancy, offering expert services in Clinical Development, Data Management, Clinical Program Management, Medical Writing, Regulatory Affairs, Medical Affairs, Pharmacovigilance, Safety Summary Documents and Bio analytics. Partner with us to advance your research projects with precision and compliance. Discover how we can support your research journey today.
Our Services
Being in AI era
AI-Powered Clinical Research Solutions
We are in the process of developing AIdriven dashboards for the next generation of clinical research, enabling you to:
Optimize trial recruitment with real-time candidate tracking
Accelerate data analysis via automated workflows
Uncover actionable trends and deep insights
Therapeutic areas
Expert clinical research consulting across key therapeutic areas: Oncology, Immunology, Cardiovascular, Neuroscience, Ophthalmology, Infectious Diseases, Metabolic Disorders, Renal and Dermatology.
Pushing the boundaries of modern medicine, our expertise includes gene therapies and radioligand treatments.
Clinical Development
Expert guidance and management through all phases of clinical trials to ensure regulatory compliance and successful study outcomes.
Clinical Program / Project Management
Project management and operational support, strategic inputs to the drug development including budgeting, global and regional submission plans.
Clinical Data Management
Accurate and efficient data collection, validation, review and analysis to support clinical research integrity and reporting.
Bio-Analytics
From bespoke analytical method development and full-scale validation to smooth protocol transfer and in-depth stability & compatibility assessments, we deliver regulatory-ready data you can trust
Early Development
Combining BABE, PK, and PD expertise, we provide actionable insights that accelerate your go/no-go decisions.
Medical Writing
Study Planning: IB, Protocols & ICFs.
Safety & PV: Aggregate DSUR, PBRER/PSUR, RMP, Signal Management, & ICSR narratives.
Clinical Reporting: CSR, Plain Language Summaries (PLS), & redaction support.
Global Submissions: Expert authoring for CTD/eCTD Modules 2 & 5, ready for publishing.
Regulatory
We provide end-to-end documentation support for the entire drug development lifecycle, ensuring global compliance (ICH, FDA, EMA) and audit-readiness.
Pharmacovigilance
Monitoring and evaluation of drug safety to ensure patient safety and regulatory adherence throughout product use.
Biostatistics
Advancing health through precise clinical innovation and insight.
Partner with us for excellence!
Team
Gokul Pallempati
Gokul is a clinical development expert with over 14 years of experience in global pharmaceutical and biotech companies. He specializes in clinical data analysis, clinical research trends & insights, regulatory document preparation, and medical affairs, with a strong focus on ophthalmology. Gokul has led and supported numerous clinical programs, combining scientific rigor with strategic insight to drive successful clinical research outcomes and improve patient care.
With a strong foundation in evidence-based medicine and a commitment to patient-centric development, Gokul continues to drive innovation and excellence in clinical research and medical affairs.
Karthekeyan Subramanian V
With over 16 years of experience in pharmaceutical analysis and development, Karthekeyan Subramanian V brings deep expertise in analytical method development, validation, and method transfer to FDA-approved manufacturing facilities. He has a strong background in analytical equipment validation and experimental design, and is highly skilled in conducting stability and excipient compatibility studies across various dosage forms, including tablets, capsules, oral suspensions, nasal sprays, creams, injections etc. His work ensures regulatory compliance and supports robust product development across diverse pharmaceutical matrices.
His Specialties:
Analytical Method Development | Method Validation | Method Transfer | Stability & Compatibility Studies
Uday Kumar Jammula
Clinical Data Management Specialist With a strong foundation in regulatory compliance and technical execution. Uday oversees the full lifecycle of clinical data to ensure integrity and timeliness. Expertise includes coordinating Case Report Form (CRF) design, implementing Electronic Data Capture (EDC) systems, and executing rigorous User Acceptance Testing (UAT). Uday is dedicated to developing robust SOPs and data standards that align with ICH-GCP, HIPAA, and US DHHS guidelines, ensuring every trial meets the highest quality benchmarks from study planning to database lock.