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When deciding on a QPPV partner, it's crucial to opt for one with access to top-tier local specialists and the ability to offer adaptable, tailor-made solutions for precise requirements. Navitas Life Sciences delivers comprehensive and seamless solutions encompassing QPPV responsibilities and extending to comprehensive safety reporting management, ...
What is Medical Writing? Medical writing is the creation of meticulously structured scientific documents, spanning a range of materials including clinical research documents. Regulatory medical writing involves the structured crafting of documents intended for submission to regulatory agencies seeking approval for medical devices, drugs, and biolog...
IDMP compliance, whether it's for UCSF IDMP, EU IDMP, or FDA IDMP, requires comprehensive solutions tailored to your organization's unique needs. At Navitas Life Sciences, we specialize in providing expert guidance and support to ensure seamless adherence to IDMP standards and guidelines. Our solutions encompass every aspect of IDMP compliance, inc...
World Cancer Day 2024 is celebrated to bring awareness to a global health crisis claiming around 10 million lives annually. As the world copes with the rising burden of cancer cases, the landscape of cancer research is witnessing transformative innovations. What is a Clinical Trial for Cancer? A clinical trial for cancer is a carefully designed res...
Navitas Life Sciences provides the right platform for clinical research excellence, where innovation meets precision. At Navitas Life Sciences, we're at the forefront of revolutionizing clinical research management systems, collaborating seamlessly to drive efficient biosimilar clinical trials to be among the leading pharma CROs. “We found N...
Generative AI in clinical trials, a subset of Artificial Intelligence (AI), holds promise as clinical trials not only should be flexible and adaptable but also cost-effective, catering to the diverse needs of various stakeholder groups. The intricacies of clinical trials, inherently labor-intensive, complex, and heavily regulated, make this task pa...
Clinical Research Organizations (CROs) play a significant role in clinical research and in transforming healthcare. Ranging from catering to specialized niche pharmaceutical companies to expansive global pharma companies, CROs serve as the driving force behind the journey of new drugs and medical devices from conception to FDA approval. CRO’...
Clinical trials present a complex landscape that demands meticulous navigation through the intricacies of protocol development, regulatory compliance, and trial management—an inherently formidable task. It is in this intricate terrain that Contract Research Organizations (CROs) assume a pivotal role, emerging as indispensable partners for sp...
In this exciting blog, we focus on the research and innovation in rare disease clinical trials. Navitas Life Sciences’ commitment to accelerating pharmaceutical breakthroughs globally is reflected in our extensive experience of 600+ clinical trials, expertise in 20+ therapeutic areas, and a proven track record of collaborating with biopharma...
The World Health Organization states that nearly 39 million people live with HIV/AIDS globally (2022), with 630,000 people dying due to HIV related causes, necessitating the need for improved treatment and care. Navitas Life Sciences has been supporting the efficient management of clinical trials for small to large pharma and life sciences companie...