VivoClin Research Services is at the forefront of advancing clinical research with precision and expertise. We specialize in comprehensive clinical trial site support and medical writing, ensuring meticulous execution and high-quality research that drives medical innovation. With dedicated operations across regions, including our Australia division, we continue to expand our global impact in pharmaceutical and clinical research.
Comprehensive site management for clinical trials
High-quality scientific and regulatory documentation
End-to-end assistance for research projects
A team committed to driving innovation and excellence in healthcare.
Dr. Kunal Maheshwari is an experienced medical writer and clinical research professional with expertise in scientific writing, regulatory documentation, and medical communications. His proficiency in crafting high-quality manuscripts, clinical study reports, and regulatory submissions ensures clarity, accuracy, and compliance with industry standards. With a strong background in clinical research, he bridges the gap between scientific data and effective communication, contributing to impactful medical literature and research excellence.
Dr. Mohammad Kaif is an experienced clinical research professional with expertise in study coordination and quality assurance. As a scientific writing expert, he has contributed to impactful research through numerous authored manuscripts. His multidisciplinary experience strengthens clinical trial execution and regulatory compliance.
Dr. Gopal Natesan is a distinguished pharmaceutical scientist with expertise in clinical research, medical writing, and regulatory sciences. With over two decades of experience, he has contributed to scientific communication, quality assurance, and research excellence. As the Director at Nirma University, Ahmedabad, he plays a key role in fostering industry collaborations and academic advancements. His expertise strengthens our commitment to high-quality research and regulatory support.
Dr. Humzah Postwala, Pharm.D, is an expert in medical writing, clinical research, and the pharmaceutical industry. Having cleared OPRA in Australia, he combines academic excellence with industry experience to advance evidence-based practices and scientific communication. As Head of the Australia Division, he leads strategic operations, fosters partnerships, and drives the organization’s growth in the Australian pharmaceutical and clinical research sector.
Dr. Hardik Pitroda is an experienced dermatologist with over a decade of expertise in patient care. As a principal investigator in numerous clinical trials, he has contributed to advancements in medical science and therapeutic innovations. His deep understanding of clinical trial methodologies, regulatory compliance, and investigational treatments strengthens our research capabilities. With a strong commitment to evidence-based medicine, Dr. Pitroda plays a key role in ensuring the success and integrity of clinical trials.