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The International Clinical Trials Day brought to the fore the significance of Clinical trials in supporting medical advancements. Clinical Trials provide the necessary data to bring new treatments to the market. Contract Research Organizations (CROs) play a pivotal role in this process, offering comprehensive support for the planning, execution, and management of these trials.
A Clinical Trials CRO provides comprehensive support to pharmaceutical, biotechnology, and medical device industries for the planning, execution, and management of clinical trials. These organizations handle various aspects such as study design, patient recruitment, data management, regulatory compliance, and biostatistics. CROs are vital for facilitating faster reach of drugs to the market, ensuring compliance with regulatory standards, and enhancing the efficiency and quality of clinical trials. As of 2024, several CROs have distinguished themselves in the industry for their innovative approaches and exceptional service, with some moving to top cros by revenue while some others have gained to rank among top 5 cros based on technological expertise. Navitas Life Sciences, a leading global CRO with over 30 years of experience, 600+ clinical trials across 20+ therapeutic areas is among top cros in the world.
Clinical trials improve global health by developing new treatments, enhancing disease prevention, and refining existing therapies for better efficacy and safety. They advance medical knowledge, personalize medicine by tailoring treatments to specific populations, and inform public health policies with evidence-based data. Through these contributions, clinical trials play a crucial role in controlling diseases and improving overall healthcare outcomes.
Decentralized clinical trials (DCTs) use digital technologies and remote methods to conduct clinical research. They minimize the need for participants to visit traditional clinical sites by utilizing telemedicine, mobile health apps, home health care, and wearable devices. This approach enhances participant convenience, broadens access, and can improve data collection efficiency.
Participants for a clinical trial are assembled through a multi-step process which includes inclusion or exclusion based on eligibility criteria, with the use of patient registries, and outreach campaigns. An initial screening is conducted to ensure participants meet the eligibility criteria, post which they are provided with detailed information about the trial, and written consent obtained. Qualified and consenting participants are then enrolled into the trial
Clinical trial supply involves the sourcing, manufacturing, packaging, labeling, storage, and distribution of drugs and medical devices needed for clinical trials. It ensures regulatory compliance, maintains product integrity, and supports timely trial execution.
Navitas Life Sciences stands out for its innovative solutions and commitment to efficiency. It is a knowledge-based full services CRO utilizing leading edge technology to power efficient clinical trials. Our comprehensive service offerings cover the entire clinical trial lifecycle, from planning and regulatory consulting to data management and biostatistics. Clients include the biopharmaceutical industry, foundations, academia, and the US Federal Government (including multiple institutes at the NIH, FDA, CDC, WRAIR, and DoD).
Navitas Life Sciences has carved a niche for itself by consistently delivering high-quality services that enhance the efficiency of clinical trials. Here are some key aspects that make Navitas Life Sciences feature among the top cros in the US:
Innovative Technology Integration: AI and ML
Navitas Life Sciences leverages advanced AI and machine learning based technologies such as One Clinical Analytics, that provide near real time data insights to optimize clinical trial processes. These technologies help in predictive analytics, patient recruitment, and data management, ensuring that trials are conducted more efficiently and cost-effectively.
Comprehensive Service Offerings: End-to-End Clinical Trial Support
From early-phase development to post-marketing surveillance, Navitas Life Sciences offers a full spectrum of services. This includes regulatory consulting, pharmacovigilance, data management, and biostatistics. Our holistic approach ensures seamless transitions between different phases of clinical development.
Global Reach and Local Expertise
With a presence in multiple countries, Navitas Life Sciences combines global reach with local expertise. This enables them to navigate regulatory landscapes effectively and recruit diverse patient populations, enhancing the robustness of clinical trial data.
Patient-Centric Approach
Navitas Life Sciences places a strong emphasis on patient engagement and retention. By utilizing digital tools and patient-centric designs, they ensure higher enrolment rates and better patient adherence, which are critical for the success of clinical trials.
In 2024, the landscape of clinical research is shaped by organizations that blend innovation with efficiency. Navitas Life Sciences exemplifies this blend, setting a high standard in the industry with its comprehensive and patient-centric approach to clinical trials. As the industry continues to evolve, we, along with other top ten cros, will play a crucial role in advancing medical research and bringing new treatments to market faster and more efficiently.
Date: 29th – 30th May 2024
Venue: Kohinoor Continental Hotel, Mumbai, India.
Navitas Life Sciences is pleased to be attending the upcoming 15th Annual Clinical Trials Summit 2024 scheduled from May 29th - 30th, 2024 at Kohinoor Continental Hotel, Mumbai, India.
Why do Top Pharma love our Patient Centric Trials? Book an exclusive conversation with our team at the 15th Annual Clinical Trials Summit 2024 for key insights.
Schedule you Meeting here.
Thirumalaivasan K
Assistant Vice President – CDO
Nidhi Acharya
Senior Manager - Business Development
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