Identifying the Right Investigators and Patients for your Study – Mini Podcast Biosimilar Development Capabilities – Watch Now Vaccine Development Capabilities - Brochure Check out our latest Validated PK & ADA Methods List Read about Veeda's partnership with Ahammune Biosciences for first in human studies Check out our Assay List (Method Library)
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A Capable,
Knowledgeable, and
Reliable Partner for
Your Clinical Trials

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16 Years of Delivering
Scientific Excellence

Through Safe and Quality Research
Solutions with No Compromise on
Ethical Practices

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Enabling Healthcare's
Ambition

Of Longer, Healthier and
Happier Lives

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Driven by Knowledge
and Experience

To support diverse drug
development programs through
comprehensive service capabilities

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Entrusted by
Lifesavers Worldwide

A trusted partner to 10 of the
world's top 15 Global Generic
Pharma Companies

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A Full-Service Independent Asia Pacific Based CRO

Veeda Clinical Research Limited (“Veeda”), an Independent Asia Pacific Based CRO, together with its subsidiary, Bioneeds India Private Limited (“Bioneeds”), and its joint venture, Ingenuity Biosciences Private Limited (“Ingenuity”), (together referred to as the “Veeda Group”) offers a comprehensive portfolio of clinical, preclinical and bio/analytical services to support innovator, biosimilar and generic drug development programs of our UK-based clientele.

We are an independent, institutional investors owned, Board governed, and professionally managed contract research group offering scientific leadership, global quality management systems, and long-term operational and financial stability through continuing investment in our people, processes, systems, infrastructure, technology, and a deep commitment to quality.

Together, we serve clients globally in the following industries:

● Pharmaceutical and Biopharmaceutical
● Agrochemical and Industrial Chemicals
● Herbal/Nutraceuticals
● Medical Devices

A Reliable Clinical Research Partner to the Pharma Fraternity

The success of a clinical trial is driven by the strategic selection of a reliable Clinical Research Organization (CRO). Our vastly experienced team of highly qualified professionals, a comprehensive portfolio of clinical research services to support diverse requirements, and a robust Quality Management System guided and nurtured by our quality culture makes us a partner of choice for some of the leading pharmaceutical companies in the world.

Advancing Human Life with Scientific Excellence & Constant Innovation

Medical science is on a constant quest to develop better and more effective treatments, prevent diseases, and provide accurate cures to human life. We aim to be a catalyst in this quest of advancing medical science forward.

We strongly believe in scientific excellence through teamwork, and this has helped us rise to become one of the most competent partners for the (Bio) pharmaceutical companies across the globe.

Veeda constantly strives to be a partner for the pharmaceutical world by bridging the gap of bringing a therapy from Lab to Shelf, thereby contributing towards achieving the human ambition of having a longer, healthier, and happier life.

Our Broad Range of Specialized Services

Pre Clinical Research
and Development

Offering cutting edge Drug Discovery and Development services to support medicinal chemistry, biology, toxicology, Process R&D, formulation, analytical development and more.

Bioavailability & Bioequivalence (BA/BE)

Helping pharmaceutical companies accelerate their regulatory submission and drug approval applications with our regulated bioequivalence and bioavailability studies.

Bio Analytical

Offering a full range of Bio Analytical Services supporting various aspects of the drug discovery and development to understand and estimate the complexity involved during execution.

Early Phase Clinical Development

Managing early phase clinical trials safely and efficiently in healthy volunteers & patients.

Late Phase Clinical Development

Offering comprehensive services for Phase II-IV clinical trials along with feasibility studies, regulatory submissions, site management, data management and more.

Bio-Pharmaceutics & Data Science

Delivering robust analysis and reports to ensure that projects stay on track, on time, and within budget.

Large Molecules & Biosimilar Development

Solving complex large molecules, including vaccines, novel biologics, and biosimilar challenges with access to fully integrated end-to-end development services, delivered with quality, flexibility, and speed.

Post Marketing Surveillance

Offering broad spectrum of high quality, flexible, cost effective and scalable safety monitoring services that can fit seamlessly into your process.

Veeda has experience of handling studies in various therapeutic segments

Oncology

Your Trusted Partner for Oncology Clinical Trials

Overcoming the complexity in oncology trials, Veeda has completed oncology, PK, and Phase II studies, while other oncology studies are at different stages of execution. Having an extensive experience in 30+ Molecules, we have recruited 900+ patients in different oncology indications.

Dermatology

Achieving your Dermatology Clinical Study objectives effectively

With a database of 75+ dermatologists with registered IEC, we provide the highest quality and efficient clinical study design for your dermatology studies. We have conducted detailed feasibilities for various dermatological products in indications like impetigo, tinea pedis, scabies, cold sore, atopic dermatitis, acne vulgaris, etc., across 50 sites. We have recruited 450+ volunteers across multiple studies that also include females-only trials, such as the estradiol transdermal system.

Ophthalmology

Providing a leading edge for all your Ophthalmology Trials Requirements

We have delivered success in clinical endpoint phase III studies of wet age-related Macular Degeneration, Uveitis, and Cataract patients with over 400 patients and 45+ active sites. With a database of 80+ Investigators comprising of retinal specialists and ophthalmologists, we are your trusted partner for any ophthalmology trial requirements.

Rheumatology

Think Rheumatology. Think Veeda

At Veeda, our rheumatologists understand and treat a myriad of diseases in this area. Our therapeutic experts can support programs in rheumatology with knowledge gained from past programs with similar populations, therapies, and investigative sites.

Gastroenterology

Your Preferred CRO for Gastroenterology Clinical Trials

At Veeda, we understand gastroenterology and complex study and protocol designs across multiple indications. We offer extensive expertise in the gastrointestinal therapeutic area of clinical trials with experience of Phase I/II PK or PD studies involving drugs acting systemically or locally in the GI tract.

Cardiology

Bringing your Cardiology Clinical Trials to Life

Our experience spans across a wide range of cardiology indications, including arrhythmias, hypertension, dyslipidemias, and congestive heart failure. We have sites equipped with telemetry and staffed by a trained cardiac team with an excellent track record in executing cardiovascular clinical studies.

ENT

Advancing Healthcare with ENT Clinical Studies

Our clinical trial team is equipped with an experienced Investigator database for conducting ENT studies across hearing and balance disorders. With a focus on ENT indications, we bring clinical knowledge with operative excellence to the design of your clinical trials and work towards creating a healthier tomorrow.

Gynaecology

Creating a Healthier World for Women with Gynaecology Studies

Veeda's team has experience of working on many clinical and Phase trial projects of women's health, including Gynaecology. Our expertise in relative indication with a robust Investigator database and Patient pool across India provides our clients with quality and delivery in the required timeline of trial data. We are your CRO partner of choice for full-service clinical trial design and execution for Gynaecology studies.

What Makes Veeda Special?

Special focus on training our employees with a Continual Development Program (CDP) to keep them equipped for new challenges in the clinical research industry.

Right blend of clinical experience in transition activities, planning, and documentation while upholding ethical values, good clinical practices, and regulatory compliance all the way.

Our ISR (Incurred Sample Reanalysis) data is >95% which is far above the USFDA recommended rate of 67%.

High throughput timelines with a history of recruiting patients for rare indications like SCLC & RCC, we aim to establish high subject recruitment, retention ratio and enhance site productivity.

Committed to providing quality research solutions that meet the requirements of sponsors & regulatory authorities while being mindful of the safety & well-being of the study volunteers

Patient Safety at the Core of Our Trials

The clinical research industry has come a long way from viewing patients as mere “subjects” to playing an integral part in the success of clinical trials. Subject and Patient safety are of utmost importance for Veeda, and we take all measures in terms of infrastructure and resources to ensure the same.

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Veeda Insights

Case Study

Bioequivalence of Brinzolamide & Brimonidine

Case Study

Euglycemic Clamp Study

Webinar

Challenges & Solutions: Development and Validation of Abatacept Biosimilar Clinical Assays

Brochure

Our Capabilities in Complex Generics

Life at Veeda

The most valuable asset of an organisation is its human talent, and at Veeda, we cherish our culture of diversity and inclusion. Our aim is to create an unparalleled Employee Value Proposition through innovative Learning and Recognition initiatives that put our employees at the center of everything we do.

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What our Clients say about us?

In a highly regulated environment, such as the pharmaceutical industry, where quality is critical and time is precious, having a trustworthy partner is one of the key elements of success. Working with Veeda provides a peace of mind with respect to consistently and timely delivering quality work. I’ve worked with Veeda on several projects and plan to continue doing so for the foreseeable future.

-Our Esteemed Client from Europe

When it comes to choosing your partner for a clinical program, Veeda is the first CRO you can think of. All these years of partnership with Veeda, we came across with high qualified personnel, fully-dedicated to our challenging demands.

-Our Esteemed Client from Europe

It has been a pleasure having Veeda CR as a contract research organization for the conduct of our bioequivalence studies. Being an independent CRO, it is good to see Veeda have a wide range of analytical methods and good clinical experience. Their quality practices, open communication, and timely delivery have been a highlight of their work system, which enables us to stay on top of our projects. Looking forward to see the good work continue in the coming years.

-Our Esteemed Client from India

As a Sponsor in a different time zone (USA), I have found Veeda Team to be very responsive in providing timely operational updates to enable our team to make quick decisions.

-Our Esteemed Client from USA

The excellent project management and support, and openness from an experienced, well-trained, and scientifically oriented team, along with the quality of the deliverables, are some of the reasons that kept us close partners, for more than 12 years. Congratulations, and keep up with good work, Veeda team!

-Our Esteemed Client from Europe

Our organization has worked with Veeda for a number of years, and we are continually impressed with the team’s speed of responsiveness to their customers.

The Veeda team is available, knowledgeable, and always willing to work through any queries we might have. We greatly value Veeda’s customer service, expertise, and seamless project management. Congratulations on 15 years of Clinical Excellence!

-Our Esteemed Client from USA