“Why WHO-GMP Certification Matters in Pharmaceutical Manufacturing”
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Daundi Biological Pvt. Ltd. is a progressive pharmaceutical company established in 2024, dedicated to developing and manufacturing high-quality pharmaceutical products. With state-of-the-art manufacturing facilities built to meet PIC/S, WHO-GMP, and Indian regulatory standards, we uphold global compliance and excellence. Our NABL- aspiring labs and innovative R&D center facilitate product development, bulk and finished product testing, and stability studies, thereby fostering continuous innovation in healthcare solutions.
We follow a zero approach to quality rigorous testing at every stage.
We believe in long-term collaborations transfer with full regulatory support.
Innovation fuels our growth from our NABL aspiring lab to our product development.
At Daundi Biological Pvt Ltd, we integrate scientific precision with rigorous regulatory compliances , following revised schedule M Guideline , cGMP and GLP Guidelines to international regulatory standards to produce high pharmaceutical products, thereby ensuring the future of global healthcare.
Facility Overview
Daundi Biological Pvt. Ltd. operates with two primary blocks: a manufacturing block and an R&D block. The manufacturing unit specializes in producing a wide range of pharmaceutical formulations including solid oral dosages (tablets, capsules, granules, powder), oral liquids (syrups, suspensions, sachets), external preparations (solutions, creams, ointments, emulsions), and parenterals (liquid vials and ampoules). The R&D block is dedicated to Analytical Research & Development (ARD), Formulation Research & Development (FRD), and is aligned with NABL standards for laboratory operations, supporting innovation and quality assurance.
At Daundi Biological Pvt Ltd, we bring integrity, innovation, and international compliance to every formulation. As your reliable partner in pharmaceutical and biotechnology manufacturing, we are committed to delivering safe, effective, and high-quality solutions that power global health.
Our facility is designed to comply with PIC/S, WHO-GMP ensuring your products meet global quality expectations.
Get full support with regulatory filings, batch traceability simplifying audits and exports.
Here’s what our valued partners have to say about working with us—first-hand experiences that reflect our dedication to excellence in pharmaceutical manufacturing and research.
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