Full Service
Clinical Trials

Your partner for end-to-end Full-service clinical trials

End-to-end
Clinical Research Capabilities

Learn more about how we can support your decentralized clinical trials by leveraging technology & analytics

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!

Your partner for end-to-end Full-service clinical trials

We support your aspirations to bring life-saving medicines to market through well-managed clinical trials. With over 30 years of experience in conducting clinical trials, we understand your key challenges and have established systems to run a successful trial. Right from phase I to phase IV, we support your organization from startup to closure, and beyond, with our regulatory insights and quality approach. Our services are backed by technology & analytics that are developed specifically to meet the challenges you face daily, giving you the competitive edge.

Navitas Life Sciences

is named as a Major Contender
in Everest Group’s

Clinical Development Platforms Products
PEAK Matrix® Assessment 2022

The Navitas Life Sciences Guarantee

Patient Centricity

Patient Centricity

Ensured Compliance

Ensured Compliance

Assured Quality

Assured Quality

Improved Collaboration

Improved Collaboration

Cost Optimization

Cost Optimization

Navitas Life Sciences leverages its domain expertise, technology knowledge, and world-class systems & processes to support your needs. Our end-to-end clinical trials operations provide you support with Clinical program management, feasibility, site selection and activation, Site management and clinical monitoring (including Risk Based Monitoring (RBM), Central Monitoring (CM), Remote Monitoring (RM) & Adaptive monitoring). We also offer you the advantage of our expertise in Medical Imaging, Bioavailability & Bioequivalence (BABE) studies, Bioequivalence pharmacokinetic (BE PK) and Bioequivalence clinical endpoint (BE CE), Biosimilars, and Non-Interventional Studies (NIS).

Comprehensive Clinical
Trials Services

Clinical Program Management

Feasibility, Site Selection & Activation

Site Management & Clinical Monitoring (RBM, CM, RM & Adaptive)

Specialized Clinical
Expertise

Biosimilars

Non-Interventional Studies

Real World Evidence

Deep Domain Expertise

Navitas Life Sciences has supported over 600+ Clinical Trials covering 140,000+ patients across 20+ theraputic areas.

Extensive Therapeutic Experience

We have supported clinical trials across 20+ therapeutic areas including Oncology, Haematology, Neurology and much more.
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Oncology / Hematology

Acute Myeloid Leukemia, Blood Cancer, Brain Tumor / CNS Lesions, Breast Cancer, Colorectal Cancer, Follicular lymphoma, Liver Disease   NSCLC, Prostate Cancer, Skin Cancer

Dermatology

Atopic Dermatitis, Onychomycosis, Psoriasis

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Endocrinology

Diabetes Foot Ulcer, Type II Diabetes

Respiratory

Asthma, Chronic Obstructive Pulmonary Disease, Cough, Idiopathic Pulmonary Fibrosis, Interstitial Lung Disease, Respiratory Tract Infection
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Gastrointestinal (GI)

Anal Fissure, Chronic Idiopathic Constipation, Gastrointestinal Tract, Liver Disease, Ulcerative Colitis / Crohn’s Disease

Cardiology

Acute Myocardial Infractions, Congestive Heart Failure, Critical Limb Ischemia, Coronary Artery Disease

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Neurology

Alzheimer’s Disease, Cerebral Stroke, Dementia, Multiple Sclerosis, Parkinson’s Disease

Immunology / Vaccines

Allergic Asthma, Allergic Conjunctivitis, Allergic Rhinitis, Allergy, Chronic Thrombocytopenic Purpura, Hepatitis B Liver Transplanted Patients, Psoriasis (anti-metabolite), Renal Transplantation with Immunosuppressant Therapy, Infant Vaccination

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Other therapeutic areas

Mental health, Musculoskeletal diseases, Neurology/CNS and infectious diseases

Get in touch

On time, High quality clinical trial for oncology

At Navitas, we understand the complexities of an oncology clinical trial and have vast experience and technical know-how, along with quick onboarding and award-winning recruitment process to complete your trial.

Oncology case study

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

Rapid data integration

AI driven platform allows rapid data integration with near real time data insights
Faster and informed decision making

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

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
Informed Decisions
Proactive Action
Proactive Action
Successful Outcomes
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