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Pharmacovigilance automation holds considerable potential for large-scale transformation, particularly during a period of heightened emphasis on safety and the reporting of adverse drug effects—fundamental aspects of pharmacovigilance. This automation represents a potent tool for enhancing literature search in pharmacovigilance, revolutioniz...
In this blog, three seasoned experts share their insights and expertise regarding the growing significance of patient clinical registries and their pivotal role in building our healthcare systems. Dr Yun Lu, boasting decades of experience in developing and managing patient registries, serves as the Chief Science and Innovation Officer at Navitas Li...
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...
The clinical trials ecosystem is undergoing a transformative shift in 2024, fueled by technological advancements, regulatory updates, and an increasing focus on patient-centricity. As medical research continues to evolve, it is crucial to stay informed about the latest trends in clinical trials shaping the field. In this blog, we delve into the top...
Navitas Life Sciences joins The World Health Organization in raising awareness about cervical cancer this January, Cervical Cancer Awareness Month. According to the WHO, 604,000 were affected with cervical cancer globally in 2020, and it is the fourth most common type of cancer. In the UK, around 3,200 new cervical cancer cases are identified every...
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...