We’re deeply committed to supporting biotech, pharma & research institutes on their quest to develop ground-breaking new therapies. T To do this, we offer a comprehensive suite of clinical solutions across diverse therapeutic areas from the early stage to the development phase. We draw upon our extensive experience across multiple geographies to deliver customized and tailored approaches that meet the unique needs of each client.
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We specialize in testing the safety and efficacy of a new drugs and diagnostic tests in humans.
Learn moreOur services, backed by our experience, provide clarity, accuracy, and accessibility in medical communication.
Learn moreOur team partners with CROs/Sponsors to create a clinical trial strategy that aligns with their product’s unique requirements. We utilize a collaborative approach to plan clinical procedures at the hospital or clinical trial facility, ensuring a successful clinical trial by obtaining regulatory clearances and setting the stage for a smooth clinical trial process.
We serve as the primary liaison between the CRO/sponsor, ethics committees, regulatory bodies, vendors, and healthcare facilities, working to create a cohesive and streamlined process for the establishing of a clinical study. We orchestrate communications, meetings, and reporting mechanisms to keep everyone informed of the project’s progress.
We execute clinical trials with precision, following the protocol and ethics committees’ guidelines. Our team develops meticulous monitoring procedures, ensuring that all clinical trial data is accurately recorded and documented. We leave no stone unturned to generate trust in the clinical trial process and provide regulatory authorities with the necessary data.
Our team assists in the management of clinical trials, from proof-of-concept to pivotal trials, continuously optimizing the process to ensure smooth and efficient operations. We maintain consistency and quality throughout the process’s lifetime, identifying and mitigating risks, managing budgets, delivering final clinical study reports, and ensuring all regulatory requirements are met.
We handle all aspects of regulatory and compliance activities, patient recruitment and data collection, and specialize in supporting study start-ups, monitoring, and closeout. We cater to the unique needs of each research site and clinical investigator and handle your clinical trial’s operational and administrative aspects. With NIOS, it’s easy to focus on what you do best – advancing medical knowledge and improving patient outcomes.
The pharma industry is continuously evolving, and so is CROs’ role, reach and capabilities. Dive into the details through our insightful blogs.
Contact us for perfect execution of the next trial and experience the difference expertise makes.
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