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Research and Development
RESEARCH & DEVELOPMENT

Science-Led Innovation for a Healthier World

Building on four decades of manufacturing expertise, Dano is investing in the next generation of immunological and biological products to address global public health priorities.

FOCUS AREAS

Where We Are Investing

Dano's R&D strategy is focused on high-impact vaccine and biological categories aligned with global public health priorities.

Bacterial Vaccines

Expanding our proven toxoid platform beyond Tetanus — developing combination and single-antigen products targeting Diphtheria, Pertussis, and other priority bacterial diseases for EPI and UIP programmes.

Combination Vaccines

Developing multi-antigen combination formulations — including Td, DTP, and next-generation combinations — to reduce injection burden and improve programme compliance.

Biological Drug Products

Leveraging our integrated DS+DP infrastructure to develop sterile biological drug products for proprietary and CMO pipelines, with a focus on parenteral presentations.

Technology Transfer & In-Licensing

Actively evaluating and in-licensing novel vaccine technologies from international partners for local adaptation and commercialisation targeting disease areas with unmet needs.

Regulatory Science & Quality by Design

Embedding ICH Q8–Q10 principles from earliest development stages, ensuring clear and defensible regulatory pathways to CDSCO, WHO PQ, and international market authorisations.

PRODUCT PIPELINE

Pipeline Overview

Our pipeline spans the marketed portfolio and active development programmes.

Product Research Pre-clinical Clinical Registration Marketed Indication
DANO-TT®
Tetanus Vaccine (Adsorbed)
Active immunisation against tetanus
Marketed
Stage Complete
Upcoming
Note: Pipeline information is indicative and subject to change. For partnership and licensing enquiries relating to specific pipeline products, please contact info@danovaccines.com.
TECHNOLOGY PLATFORMS

Capabilities Underpinning the Pipeline

Core Platform

Toxoid Antigen Manufacturing

Deep expertise in fermentation-based toxin production, chemical inactivation, and purification of bacterial toxoids to pharmacopoeial and WHO TRS specifications.

  • Validated upstream and downstream processes
  • Compliance with I.P., B.P., and WHO TRS monographs
  • Established process for bacterial toxoids
Fill-Finish

Aseptic Fill-Finish Infrastructure

Automated sterile filling lines with flexibility for multiple vial sizes and ampoule presentations, supporting proprietary and CMO programmes.

  • Automated filling — vials and ampoules
  • ISO-classified cleanrooms with validated HVAC
  • cGMP-compliant inspection and packaging
Adjuvant Systems

Adjuvant & Formulation Development

Experience with aluminium salt adjuvant systems for adsorbed vaccine formulations with ongoing evaluation of alternative adjuvant strategies.

  • Aluminium phosphate and hydroxide adsorption
  • Formulation stability studies per ICH Q1
  • Cold chain stability optimisation
Analytical & QC

Quality Control & Analytical Testing

Modern QC laboratories supporting full physicochemical, microbiological, and biological testing throughout the product lifecycle.

  • In-process and release testing per pharmacopoeial methods
  • Biological potency assays
  • Independent Quality Unit with full release authority

Interested in Co-Development or Tech Transfer?

Our Business Development team evaluates in-licensing opportunities and collaborative R&D arrangements.

Contact

Caring for Life

Whether you are looking for a partnership, need product information, or have a general query — our team is here to help.

+91 9281443266
info@danovaccines.com
Mon–Sat, 9:00 AM – 5:30 PM IST
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