About Us
A CDSCO-registered Contract Research Organization delivering ethical, regulatory-compliant clinical research across India and beyond.
Source Transcript Pvt. Ltd. is a professionally managed Contract Research Organization (CRO) headquartered in India, with operational presence in Hyderabad and Pune. Registered under the Central Drugs Standard Control Organization (CDSCO), we are dedicated to delivering high-quality, ethical, and regulatory-compliant clinical research services to the pharmaceutical, biotechnology, and healthcare industries.
With a strong commitment to scientific excellence and regulatory integrity, Source Transcript Pvt. Ltd. supports the complete lifecycle of clinical development — from early-phase studies to post-marketing research. Our team comprises experienced clinical research professionals, medical experts, statisticians, and regulatory specialists who ensure seamless execution of projects aligned with ICH-GCP and global standards.
Leveraging our presence in two key clinical research hubs, we provide access to diverse patient populations, qualified investigators, and advanced infrastructure. Our approach integrates innovation, quality, and efficiency to accelerate study timelines while ensuring patient safety and data reliability.
Our Mission
To be a trusted partner in clinical research by enabling the development of safe, effective, and accessible healthcare solutions worldwide.
Our Team
Meet Our Experts
At SourceTranscript, our strength lies in a highly skilled and dedicated team of professionals committed to delivering excellence in clinical data management and technology-driven solutions. With deep expertise across clinical operations, data science, quality assurance, and project management, our team ensures seamless execution of clinical trials with the highest standards of quality, compliance, and innovation.
Leadership Team
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Mr. Chandu Devanpally
Founder & Chief Executive Officer (CEO)
A visionary leader with extensive experience in clinical research and CRO management, Mr. Devanpally drives the strategic direction and growth of the organization. His expertise spans clinical trial execution, regulatory strategy, and operational excellence.
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Anand Rathi
Co-Founder & Managing Director
A visionary leader with extensive experience in clinical research and business strategy, Anand drives organizational growth, innovation, and global expansion initiatives.
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Swati Kurandale
Head -Clinical data management
Swati leads operational excellence across projects, ensuring efficient execution, regulatory compliance, and delivery of high-quality clinical data solutions.
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Datta Khilare
Director – AI (ClinTrack)
Datta spearheads AI-driven innovation, focusing on advanced analytics, automation, and intelligent solutions to enhance clinical trial efficiency and data insights.
Core Team
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Isha Hingmire
Quality Assurance (QA)
Ensures adherence to global quality standards, regulatory compliance, and continuous process improvement across all projects.
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Simran Belekar
Project Manager
Manages end-to-end project execution, timelines, and stakeholder coordination to ensure successful study delivery.
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Dr. Ramaswamy
Project Manager
Brings strong clinical expertise and leadership in managing complex clinical trials with a focus on scientific and operational excellence.
Data Management & Coding Team
Specializes in medical coding and data standardization, ensuring accuracy and consistency in clinical datasets.
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Pallavi Bhimbiste
Senior Coder
Expert in coding and data quality processes, supporting high-quality database outputs and compliance.
Contributes to data processing, coding, and quality checks to maintain robust and reliable datasets.
Supports clinical data coding activities with precision and adherence to industry standards.
Our Commitment
Our team works collaboratively to leverage cutting-edge platforms like eCRF, IWRS, and remote monitoring systems to streamline clinical trials, ensuring data integrity, regulatory compliance, and faster decision-making.
Together, we are committed to transforming clinical research through innovation, technology, and operational excellence.
Our Services
What We Do
A focused and integrated range of clinical research services designed to ensure efficient study execution, regulatory compliance, and high-quality outcomes.
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Clinical Operations
Comprehensive management of clinical trial activities, ensuring smooth coordination across sites, adherence to protocols, and timely study execution in compliance with ICH-GCP and CDSCO guidelines.
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Project Management
Dedicated project managers overseeing end-to-end study lifecycle, ensuring effective planning, risk mitigation, timeline management, and seamless communication with sponsors.
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Clinical Monitoring
Expert monitoring services through experienced Clinical Research Associates (CRAs) to ensure data accuracy, protocol compliance, site performance, and patient safety.
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Medical Monitoring
Ongoing medical oversight by qualified physicians to ensure subject safety, protocol adherence, and appropriate clinical decision-making throughout the study.
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Safety Management (Pharmacovigilance)
Robust safety monitoring including adverse event collection, processing, reporting, and signal detection in compliance with global regulatory requirements.
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Site Feasibility & Site Selection
Strategic identification and evaluation of qualified clinical trial sites and investigators to ensure optimal patient recruitment and study success.
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Quality Management
Strong quality systems including SOPs, audits, and compliance checks to ensure adherence to regulatory, ethical, and sponsor requirements.
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Clinical Data Management
End-to-end data management services including database design, data entry, validation, and query resolution to ensure clean and reliable datasets.
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Electronic Portals & Systems
Implementation and management of secure electronic platforms such as EDC (Electronic Data Capture), CTMS (Clinical Trial Management Systems), and eTMF for efficient and transparent study conduct.
Partner with Source Transcript
Source Transcript Pvt. Ltd. is committed to delivering reliable, efficient, and high-quality clinical research services, supporting sponsors in accelerating development timelines while ensuring patient safety and data integrity.