About Us
Sunsecure Clinical Research Services Pvt Ltd, headquartered in Bangalore, extends a competitive edge to its clients. Our operational base in Bangalore empowers us to deliver unmatched advantages to our esteemed clientele. Our service model spans a diverse array of domains, ensuring that we cater to a comprehensive spectrum of needs within the clinical research arena.
Our multifaceted service offerings encompass site management, clinical monitoring, clinical audits, regulatory support, clinical staffing, protocol writing, clinical data management, pharmacovigilance, and a range of allied services. This extensive array of services is meticulously designed to cater to the unique requirements of our clientele.
Our clientele is drawn from a wide spectrum of industries, including pharmaceuticals, biotechnology, medical devices, ayurvedic products, nutraceuticals, and cosmetics. This diverse clientele is a testament to our adaptability and expertise across various sectors.
In addition to providing general assistance that addresses emergent requirements, we also possess specialized expertise in supporting processes that fall under FDA regulations. This expertise extends to research encompassing experimental drugs and devices, as well as preclinical laboratory studies. By providing meticulous guidance through these intricately regulated processes, we ensure our clients' compliance and success.
Partnering with Sunsecure Clinical Research Services Pvt Ltd guarantees not only a wide spectrum of services but also a depth of expertise that guides you through the intricacies of the clinical research landscape. Our commitment to excellence, regulatory compliance, and client success forms the cornerstone of our operations.
Our principles
Quality Assurance
Ethical Conduct
Collaborative Approach
Ensuring the highest standards of quality in every aspect of our clinical research services.
Adhering to strict ethical guidelines to protect the rights and well-being of research participants.
Fostering collaboration with clients, partners, and stakeholders to drive innovation and achieve research goals.
Sravani
Our Team
Founder
Sr. Consultant - Director Quality Assurance
Mr Parassuram Dhulipalla
Mr Parassuram is a highly skilled Clinical Research Quality Assurance professional and Auditor with over two decades of progressive experience in ensuring compliance with global regulatory standards, leading cross-functional teams, and implementing continuous process improvement initiatives. Mr. Parasuram possess an unwavering commitment to excellence in Clinical Research Quality Assurance (QA) and GCP/GXP QA; Mr Parasuram has an illustrious career in Quality Assurance and has equipped with a comprehensive understanding of the intricacies of ensuring compliance with GXP standards. This encompasses both early and late-phase clinical trials. His extensive hands-on experience in orchestrating global clinical trial audits - be it for Phase I, II, or III trials, or specialized audits for QM systems, GCLP compliance, Medical Devices (ISO 14155), and Computerized systems such as eCRF, eConsent, and eTMF - stands as a testament to Mr. Parasuram's unwavering dedication to achieving excellence in QA.
Beyond this, his tenure included associations with diverse organizations globally including South Africa and UAE, from NGOs, foundations, pharmaceutical manufacturers, contract research organizations to site management organizations. This vast exposure accentuates his adaptability and depth of expertise.
Furthermore, he has a great knowledge of reviewing and approving investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA), and Effectiveness Check (EC) plans and tracking till closures for quality events arising from Quality Issues, Audits, Inspections or during similar QA activities. His consistent track record of successful trial audits across the continents, be it Asia, the USA, UK, Europe, Middle East and Africa, reflects his adaptability and keen insight into regional regulatory nuances. The accomplishment that resonates the most with his ability to seamlessly blend robust QA management skills with audit risk assessments, calibration/validation, and continuous quality improvement, fostering a culture of regulatory compliance and excellence across teams.
