Navitas Life Sciences offers comprehensive regulatory services that empower pharmaceutical, biotechnology, and medical device companies to meet string...
At Navitas Life Sciences, we pride ourselves on being at the forefront of providing comprehensive medical and regulatory consulting services that help...
In the intricate world of pharmaceutical development, where the stakes are high, deadlines are tight, and precision is non-negotiable, the role of med...
Designing complex innovative protocols for Oncology clinical trials is a complex process that must balance scientific rigor, regulatory requirements, ...
Driving transformation in the drug development landscape requires more than just adapting to changes; it demands leading them. At Navitas Life Science...
As we mark Immunization Awareness Month 2024, it's imperative to spotlight the critical role of vaccines in public health and the intricate processes ...
The recent announcement by the US Food and Drug Administration (FDA) regarding laboratory-developed tests (LDTs) indicates that increased enforcement ...
The recent shift in the UK's regulatory landscape, marked by the adoption of the International Recognition Procedure (IRP) by the Medicines and Health...
At Navitas Life Sciences, we are at the forefront of providing comprehensive regulatory services that ensure compliance, accelerate time-to-market, an...
How Navitas Life Sciences grew to be a Strategic Partner for Top Pharma across the World Clinical trials are the backbone of modern medical advancemen...
The global clinical trials market, valued at USD 80.7 billion in 2023, is projected to grow at a compound annual growth rate (CAGR) of 6.49% from 2024...
By reimagining regulatory submission strategies with artificial intelligence in regulatory affairs, pharmaceutical companies can expedite timelines an...
At Navitas Life Sciences, we believe in not just advancing the frontiers of pharmaceutical sciences but also in giving back to society and academia. D...
In the fight against counterfeit medicines, the stakes are incredibly high. Counterfeit drugs pose significant threats to public health worldwide, wit...
There is an increasing focus on diversity in clinical trials, which is crucial for providing essential data on the safety and efficacy of new treatmen...
Data management services are a critical component of any clinical trial's success. For clinical research organizations, the integration of advanced cl...
The International Clinical Trials Day brought to the fore the significance of Clinical trials in supporting medical advancements. Clinical Trials prov...
“Congratulations on the PMDA approval, that is a huge accomplishment. The submission would never have been possible without your hard work and ...
Patient-centric clinical trials, which are likely to be more efficient, productive, and engaging with patients and their needs, are at the forefront o...
In clinical research, efficiency and quality are key. As the industry continues to grow, Functional Service Provider (FSP) models are gaining populari...