Rely on our expertise to support your COVID-19 clinical trials
Harness our vast Clinical Trials and infectious disease experience, infrastructure and expertise to accelerate your COVID-19 drugs to market efficiently. Partner with us to take your COVID-19 product to market quickly and effectively!
Gain with our clinical services
The Biopharmaceutical industry is undergoing a dramatic transformation, with a definite shift towards value-based, patient-centric models that deliver improved outcomes. Technology is emerging as an enabler, with companies leveraging AI and ML to address key challenges in managing and delivering clinical trials. At Navitas Life Sciences, we offer you a compelling combination of Life Sciences expertise backed by technology know-how, to enable you to better manage your clinical trials. Our innovative end-to-end offerings address your key challenges in running clinical trials and drive better outcomes throughout the drug development process.
Patient-centric and Value-based approach Delivers Better Outcomes for Your Clinical Trial
Engagement
- Better Patient Engagement
- Improved Patient Experience
Innovation
- Near real-time insights to support the trial process
- Improved transparency for better decision-making
Outcomes
- Improved patient adherence
- Operational & financial efficiencies delivered
Deep Domain Expertise
Navitas Life Sciences has supported over 550 Clinical Trials covering 120,000 patients.
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Clinical Trials
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Therapeutic Areas
Explore our Clinical Research Solutions & Capabilities
COVID-19 Clinical Trials
Navitas Life Sciences has adapted effectively to the evolving environment to rapidly mobilize insight driven End-to-End clinical trials solutions to take your COVID-19 product to successful outcomes.
Biologics & Biosimilars Studies
Get the competitive edge for your biological product
OneClinical
Faster and Smarter execution of clinical trials
Strategic Clinical Consulting
Successful strategies with data-driven insights
Full Service Clinical Trials
Your partner for end-to-end Full-service clinical trials
Non-Interventional Studies
Ensuring you gain the best from your clinical data
Clinical Data Services
Ensuring you gain the best from your clinical data
Your preferred partner for end-to-end Full-service clinical trials
Bioavailability (BA) and Bioequivalence (BE) studies are carried out for developing a new formulation or for marketing a generic drug. In order to market a generic drug, BABE studies are required for approval from health authorities like US FDA. The drug that is being tested is studied against a well- known and commercially available drug, at same concentrations and under conditions that are similar. Companies file their Abbreviated New Drug Application (ANDA) according to 505 (j) or 505b (2) to the US FDA for marketing authorization in USA. Selection of the right clinical research organization is vital for a successful market launch.
The Navitas Life Sciences Guarantee
Patient Centricity
Ensured Compliance
Assured Quality
Improved Collaboration
Cost Optimization
OneClinical
Irrespective of where we work from, you can bank on our proven OneClinical platform or your chosen platform to ensure high quality and compliant deliverables with impressive turnaround times and lower cost.
Rapid data integration
AI driven platform allows rapid data integration with near real time data insights
Faster and informed decision making
We have capabilities to ensure informed decision making as our analytics help better monitoring of work flow with roles driven triggers.
Improved operational efficiency
Seamless collaboration with vendors is made possible using proprietary Business Process Management (BPM) tools and accelerators
Gain Value from OneClinical, our AI Driven Technology Platform
All our clinical trials are backed by OneClinical, our AI&ML driven platform that offers you near real time data visibility and analytics in an outcomes-based engagement model. With OneClinical, you can make informed decisions and take proactive action to maximize the success of your clinical trial.
Informed Decisions
Proactive Action
Successful Outcomes
OneClinical Delivers Better Outcomes for You
Save Time
We have the technical expertise to drive standardization and near real time monitoring to lower cycle times
Time for Complex Study Mapping
Cycle Time to Develop Initial Interface for Data Warehouse
Overall Cycle Time
cost to develop initial Interface for data warehouse
field monitoring costs through Triggers, Reduced SDV
cost of clinical monitoring
Reduce Cost
We can drive and deliver significant reduction in total cost through people, process and technology capabilities