• Facility design and project implementation
    • Conceptual design
    • Basis of Design (BOD)
    • Facility commissioning and qualification
  • Quality Management System implementation according to WHO, EU and USFDA standards
  • Protein- Polysacchride Conjugation capability
  • Formulation Development
    • Viral Vaccines
    • Combination vaccines (recombinant protein-polysaccharide conjugate- toxoid-whole cell vaccines)
  • Polysaccharide Vaccine development
  • Development of toxoid based products
  • Development of Recombinant vaccines (yeast and bacterial host system)


Whether you are a start up or established company who is looking for crafting a business plan and strategy, project assessment for investment decisions and commercial viability, designing plants, construction and commissioning facilities. Process optimization and development, product improvements, facility upgradation, establish quality systems then BioBridge is your ideal partner.
With our knowledge, experience we match the unique needs of each client, bringing together business needs, experience, technical skills and market demands. BioBridge is an effective partner from day 1. Whether offering recommendations or serving as a sounding board for clients' ideas, we consistently help to maximize the impact and minimize the cost of services and products.
We emphasize action, accountability, and documentation, in the best interests of our clients, partners, and staff. We preserve confidentiality and privacy in every matter.


  • Enabling Clients for complying to Global Quality Standards by Strengthening and building their Quality Management Systems through systematic reviews, gap analysis, CAPA and implementation
  • Turnkey projects (Including Tech transfer) for manufacture of Human/Veterinary products (Bacterial, Viral, Polysaccharide, Conjugates, Recombinant)
  • Turnkey projects (Including Tech transfer) for manufacture of Poultry Vaccines. Access to Bulk antigens, personnel training and finished products
  • Enabling exports through a strong business network in all Emerging markets and key rest of the world countries


  • Crafting business plan and strategy. (including portfolio optimization & augmentation)
  • Project assessment for investment decisions. (feasibility studies)
  • Designing plants as per cGMP and target market NRA requirements
  • Commissioning facilities (equipment/plant etc)
  • Process optimization and development
  • Provisioning access to Technology and products to manufacture
  • Training of technical staff for cGMP
  • Due diligence and external audits
  • Validation and qualification of systems, equipment and processes
  • Establish quality systems as per EU, WHO, USFDA standards
  • Quick expansion of business in ROW-EM markets with strategic partnerships.