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How Veeda Lifesciences empowers drug development with trusted expertise

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Witness Endless Possibilities Begin Here!

Integrated

From discovery to market, we provide end-to-end CRO solutions under one roof. Our integrated approach allows us to tailor solutions specifically for you, adapting as your project evolves and grows.

Tech- Driven

Leveraging AI, our technology transforms documents into actionable analytics, streamlining study management. Our In-house systems ensure real-time tracking and insights, empowering customers with smarter, faster solutions.

Global

Partnering with us means more than just accessing services; with our presence in 9 countries and sites across 26 geographies, you gain a global ally dedicated to your success in every corner of the world.

Your Drug’s Journey from LAB to LIFE

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Post Project Feedback
Post Project Feedback
The end of one project marks the start of another. We gather your insights, open the door to new collaborations, and maintain strong connections—earning trust that brings more than 90% of our clients back.
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Need Assessment
Need Assessment
We believe precision starts with listening. Through in-depth discovery calls and feasibility assessments, we map out your study’s scope and ensure every nuance is accounted for.
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Project Kick-off
Project Kick-off
Every tailored study begins with a thoughtful plan. We launch your project by defining goals, locking timelines, and collaborating across scientific teams to create a plan that aligns with your vision. Every detail—volunteers demographic, therapeutic area, phase, and regulatory requirements—is evaluated to ensure success.
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Patient First Approach
Patient First Approach
Our patient-centric solutions aim to reduce the added layer of complexity. We focus on leveraging insights to optimize site selection, improve recruitment, and implement tailored engagement strategies that enhance the overall patient experience.
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Central Services
Central Services
A collaboration that meets all your needs—our expert team in project management, medical writing, pharmacovigilance, data science, regulatory affairs and more works together to support and manage every phase of your studies, offering you the peace of mind you deserve.

Global team of 2,100+ dedicated professionals
advancing your drug development journey

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Pre-clinical
Pre-clinical
Your molecule's journey begins here: We start with drug discovery and take you through the IND submission, delivering regulatory-compliant data and identifying compounds that are ready for the next stage.
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Clinical Development
Clinical Development
Wherever your project stands, our fully customizable, end-to-end clinical research solutions for generics, innovators and biotherapeutics—across healthy volunteers and patients—are tailored to meet your specific needs, turning your vision into reality.
Real World Evidence
Real World Evidence
Real World Evidence
Real-world data tells the true story of how treatments perform. We use Real-World Evidence to match patients to trials more accurately, speeding up recruitment while making sure therapies are safe and effective for everyone.
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Bioanalytical
Bioanalytical
Our comprehensive support covers method development, validation, and throughput sample analysis—delivering precise insights that empower confident decisions and streamline your regulatory filings.
Biopharma Icon
Biopharma
Biopharma
Efficient and scientifically grounded non-clinical testing solutions for biotherapeutics—designed to ensure safety and regulatory acceptance, while promising greater efficacy in treating complex diseases.

Your Drug’s Journey from LAB to LIFE

Global team of 2,100+ dedicated professionals
advancing your drug development journey

Feedback icon
Post Project Feedback
The end of one project marks the start of another. We gather your insights, open the door to new collaborations, and maintain strong connections—earning trust that brings more than 90% of our clients back.
Checklist Icon
Need Assessment
We believe precision starts with listening. Through in-depth discovery calls and feasibility assessments, we map out your study’s scope and ensure every nuance is accounted for.
Lauch Icon
Project Kick-off
Every tailored study begins with a thoughtful plan. We launch your project by defining goals, locking timelines, and collaborating across scientific teams to create a plan that aligns with your vision. Every detail—volunteers demographic, therapeutic area, phase, and regulatory requirements—is evaluated to ensure success.
Frist Approch Icon
Patient First Approach
Our patient-centric solutions aim to reduce the added layer of complexity. We focus on leveraging insights to optimize site selection, improve recruitment, and implement tailored engagement strategies that enhance the overall patient experience.
Central Service Icon
Central Services
A collaboration that meets all your needs—our expert team in project management, medical writing, pharmacovigilance, data science, regulatory affairs and more works together to support and manage every phase of your studies, offering you the peace of mind you deserve.
Clinic Icon
Pre-clinical
Your molecule's journey begins here: We start with drug discovery and take you through the IND submission, delivering regulatory-compliant data and identifying compounds that are ready for the next stage.
Clinical Development Icon
Clinical Development
Wherever your project stands, our fully customizable, end-to-end clinical research solutions for generics, innovators and biotherapeutics—across healthy volunteers and patients—are tailored to meet your specific needs, turning your vision into reality.
Real World Evidence
Real World Evidence
Real-world data tells the true story of how treatments perform. We use Real-World Evidence to match patients to trials more accurately, speeding up recruitment while making sure therapies are safe and effective for everyone.
Bioanalytical Icon
Bioanalytical
Our comprehensive support covers method development, validation, and throughput sample analysis—delivering precise insights that empower confident decisions and streamline your regulatory filings.
Biopharma Icon
Biopharma
Efficient and scientifically grounded non-clinical testing solutions for biotherapeutics—designed to ensure safety and regulatory acceptance, while promising greater efficacy in treating complex diseases.

Bringing Your Innovations to Life

Small Molecules

Large Molecules

Clinical Trials

Central Services

Real World Evidence

Technology at the Forefront for your Research

Leveraging advanced technology and real world data to eliminate operational redundancies and expedite clinical study workflows




Advanced systems to compile Bioanalytical study reports within 3 weeks of the last analysis

Integration of CTMS and trial builder software to reduce trial setup times, and speed up study progress trial initiation to closeout

Automated systems for sample preparation, dispensing, and analysis resulting in a 30% throughput improvement

Global Impact in Numbers

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Clinical Trials Supported

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Global Active Clients

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Sites

Driving Cancer Discoveries Together

We strive to fill the gaps of unmet medical needs and tackle new challenges head-on, to redefine cancer care. With a legacy rooted in oncology and leading the fight against multiple myeloma, we’ve become a trusted force in advancing novel therapies. Our work goes beyond trials—we're here to transform cancer treatment, turning breakthroughs into hope for patients worldwide.

8000+ Oncology Patients Enrolled

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Leukaemia

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Lymphomas

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Myeloma

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Breast Cancer

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Prostate Cancer

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Advanced Renal
Cell Carcinoma

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Ovarian Cancer

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Gastrointestinal
Stromal Tumour

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Colorectal Cancer

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Pancreatic Cancer

Stay Informed, Stay Ahead:
Insights Tailored for You

Multiple Myeloma: Opportunities and Challenges in the Changing Treatment Landscape
November 15, 2024
Webinar
Multiple Myeloma: Opportunities and Challenges in the Changing Treatment Landscape

Expert insights into the latest advancements, evolving treatment strategies, and the future of care for patients

Watch Now
Developing Liraglutide: A GLP-1 Peptide for Type 2 Diabetes Management
November 9, 2024
Podcast
Developing Liraglutide: A GLP-1 Peptide for Type 2 Diabetes Management

Take a look at the key steps we take to conduct successful studies for complex drugs like Liraglutide

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Veeda Lifesciences
November 5, 2024
Brochure
Experience the Veeda Lifesciences Advantage

From preclinical to late phase trials, Veeda Group combines advanced technology, global expertise, and agility to streamline every stage of drug development

Read More