Clinical Trials Trends for 2022 that you need to Know

As we enter 2022, clinical trials continue to forge ahead with the latest innovations and discoveries to ensure transformational healthcare for everyo...

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Top 7 Published Articles on Regulatory Services in 2021 That Reveal Deep Domain Knowledge

Navitas Life Science's rich legacy of experience and expertise helps us serve as trusted advisors and provide tailored solutions grounded in industry ...

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15+ COVID-19 Clinical Trials Conducted by Navitas Life Sciences to Support the fight against COVID-19

Navitas Life Sciences has been successfully supporting the development of therapeutic treatment towards COVID-19 through our multifaceted end to end s...

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10 Reasons to become a NETS Member

Established in 2001, our networks community is the place to discuss trends, insights, and future solutions. There is a considerable widening of the ap...

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Flexible Solutions for Gene Therapy Trials: Tailoring Transformative Care

Human Gene therapy is a technique associated with modification or manipulation of gene expression for therapeutic purposes. Luxurna was the first huma...

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How to Stay Compliant with Evolving Regulatory Changes Using SafetyREADY

Technology has revolutionized the healthcare continuum, altering patient safety worldwide, while lowering costs and time. Recent reports have estimate...

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Navitas Life Sciences Supports Effective Treatment for Respiratory Diseases with State-of-the-Art Inhalation Studies

World COPD Day 2021 was celebrated recently, and it brought with it the awareness to find better solutions for Chronic Obstructive Pulmonary Disease (...

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Supporting Diabetes Care with Efficient Euglycemic Clamp Studies

The advent of peptides and insulin analogs for the treatment of Diabetes Mellitus has enabled improved management of the disorder. The biosimilars in ...

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How Navitas Life Sciences Addresses your Regulatory Needs with Expert Regulatory Contract Staffing Services

Small to large pharmas are often faced with regulatory needs that could prolong access of their drug product to the market. Handling such requirements...

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How We go the Extra Mile to Support Your Clinical Trial Needs: 50 Sponsor Reviews You Must Read

Navitas Life Sciences remains committed to transforming clinical trials using technology led innovations, data analytics and the vast experience of ex...

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How We Remain Preferred Clinical Partners for U.S. Federal Agencies

Navitas Clinical Research (a part of Navitas Life Sciences) is a trusted partner to the US Federal Government, non-profits & academia for clinical...

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How to use Personalized Biometrics Support to Run Better Clinical Trials

It is World Statistics Day on 20th October, and we would like to highlight how effective biometric support is rising as a top strategic priority for r...

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What Makes us RISE to Support Patient Centric Oncology Clinical Trials? Supporting Breast Cancer Awareness Month

October is breast cancer awareness month, and Navitas Life Sciences continues to RISE consistently to the unique needs of oncology patients. Balancing...

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How to be Data Smart with R Programming and Accelerate Clinical Trial Efficiency

Technology led Navitas Life Sciences amped-up digital initiatives, especially during the pandemic, with the inclusion of innovation, creating fertile ...

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How to Run Successful Clinical Trials During the Pandemic and Beyond

There was a considerable change in the clinical trial landscape at the onset of the global epidemic, with the initiation of multiple COVID-19 clinical...

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How Our PV Networks Provide Vital Insights Towards Ensuring Patient Safety

Navitas Life Sciences joins the National Coordination Centre, Indian Pharmacopoeia Commission in celebrating National Pharmacovigilance week 17-23rd S...

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Gain Cutting Edge Perspective from Experts on Clinical Trial Strategy and Management

Here is how Navitas Life Sciences Defines Key Aspects on Building a resilient Future Recent publications include powerful insights from our team of ex...

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How Navitas Life Sciences helps Leading Pharma Unlock the Value of their Clinical Data

Dr. Manish Harsh, Vice President, Clinical Data Services provides key insights about the impact of technology on efficient clinical data management Th...

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Why is it Advantageous to outsource QPPV to Navitas Life Sciences?

All about QPPV with Dr Philipp Hofmann, Head of Pharmacovigilance, QPPV, Navitas Life Sciences A Market Authorization Holder (MAH) appoints a Qualifie...

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How pharmaREADY® is Driving Transformation in Regulatory Affairs

Celebrating 200+ pharmaREADY® customers and 100% satisfied users Marty Boom, Global Head of Regulatory and Safety,Navitas Life Sciences “T...

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