Partner with Veeda Lifesciences to transform your breakthrough science into approved therapies. Our comprehensive platform seamlessly integrates everything under one roof. With 20+ years of experience and a track record of regulatory success, we bring deep scientific expertise and cutting-edge technology to every project.
Our dedicated teams work as an extension of yours, providing flexible solutions that adapt to your unique needs, from targeted support to complete development programs. By eliminating traditional handoffs and delays, we accelerate your development timeline while maintaining the highest quality standards.
At Veeda Lifesciences, through our subsidiary Bioneeds, we offer top-notch preclinical research services backed by over 16 years of experience. As an OECD GLP-certified and USFDA-audited CRO, we've successfully submitted over 23,500 GLP studies to global regulatory authorities. With state-of-the-art facilities near Bangalore and a dedicated Synthetic Chemistry lab in Peenya, our team of 400+ experts is here to provide seamless, integrated solutions throughout your drug development lifecycle.
Your breakthrough science deserves a partner who can match your ambition. We specialize in Assay Biology and ADMET/DMPK solutions, offering a comprehensive range of in vitro assays tailored to support your research and integrated drug development efforts. Our assays are designed to meet the specific needs of your projects, whether you require stand-alone research support or a more integrated approach to drug development.
Veeda Biopharma’s Bioprocess Development Division excels in developing therapeutic and non-therapeutic proteins using microbial (E. coli) and mammalian (CHO; HEK) systems. We ensure development of high yielding stable clones with full traceability. Starting at microbioreactor level, we scale up at 5 L with capacity to expand to 50 L SU bioreactor, adhering to GMP and GLP standards.
Veeda Biopharma offers cutting-edge analytical solutions for structural and functional product characterization and comprehensive Analytical CMC support. We provide biopharmaceutical organizations with crucial data and insights for product advancement. Utilizing state-of-the-art technologies, our expert team ensures efficacy, safety, and regulatory compliance, driving innovation and achieving strategic goals.
Veeda Biopharma provides comprehensive large-molecule bioanalytical services for early and late-phase clinical trials, delivering precise data through advanced technology and rigorous quality assurance. Adhering to GCP and GLP standards, our expertise ensures accurate, efficient analysis, enabling well informed decisions for successful biotherapeutic development programs.
With over 30 scientists and a proven track record, our Veeda Biopharma team excels in developing biosimilars and biologics for global clients.
Integrating all stages from discovery to market under one roof, ensuring a streamlined experience for clients.
Fostering strong relationships through a collaborative, flexible approach, we offer standalone or comprehensive solutions tailored to meet all client needs.
Our infrastructure combines the latest advancements and modern facilities to deliver exceptional precision and performance.
Enforcing stringent quality control measures throughout every phase of our studies to ensure the accuracy, reliability, and regulatory compliance of all data and results.
Capitalize on our cost-efficient operations in India for affordable, high-quality solutions.
Attractive partner for both large pharma and mid-sized biotech companies globally.
A unified global network delivering seamless, end to-end solutions through dedicated arms, ensuring value and synergy for clients worldwide.
Discover how to achieve biosimilarity with precision and compliance
Guiding our clients through each stage of Biosimilar development efficiently
Peptides, Oligonucleotides, Insulin & Analogs, Fusion Proteins & Recombinant Proteins, mAbs, ADCs