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
Leadership Team
Our strength lies in our experienced and dedicated leadership team, bringing deep expertise across clinical research, operations, and data sciences.
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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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Mr. Anand Rathi
Co-Founder & Managing Director
Mr. Rathi plays a key role in overseeing business operations and corporate strategy. With strong leadership and industry insight, he ensures organizational efficiency and sustainable growth.
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Ms. Swati Kurandale
Head, Data Management
An expert in clinical data systems and processes, Ms. Kurandale leads the data management function, ensuring high-quality, compliant, and reliable clinical data across all studies.
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Ms. Simran Belekar
Project Manager
Ms. Belekar is responsible for end-to-end project execution, ensuring studies are delivered on time, within scope, and in compliance with regulatory standards.
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Mr. Ramaswamy
Project Manager
With strong operational expertise, Mr. Ramaswamy manages clinical projects with a focus on efficiency, quality, and seamless coordination between stakeholders.
Together, our team combines scientific expertise, operational excellence, and a commitment to quality, ensuring successful delivery of clinical research projects and building long-term partnerships with our clients.
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.