Innovations in bioprocessing, formulation & stability of vaccines are redefining how vaccines are manufactured, preserved, and delivered globally. From cell culture optimization to downstream purification, every stage of vaccine production demands precision and consistency. Stabilizing agents and novel excipients are being integrated to extend shelf life and maintain potency in diverse storage conditions, particularly important for low-resource settings. Lyophilization, microencapsulation, and thermostable formulations are among the promising strategies ensuring stability without relying on cold chain infrastructure. Quality by design (QbD) principles and real-time monitoring technologies are also helping manufacturers maintain rigorous standards. As vaccine technologies evolve rapidly, optimizing bioprocessing, formulation & stability of vaccines is critical for cost-effective, scalable, and equitable immunization programs worldwide.
Title : A promising novel approach to DNA vaccines
Khursheed Nadeem Anwer, IMUNON, United States
Title : Nanoscopic SubATVax™ adjuvanted vaccines against influenza A types H3N2, H1N1 and influenza type B for subcutaneous administration
David Craig Wright, D4 Labs, LLC, United States
Title : The importance of post-marketing surveillance and real-world data for a product to be successful
Regina Au, BioMarketing Insight, United States
Title : Prophylactic and molecular approaches for mitigating human influenza A viruses: i. Evaluating influenza vaccine effectiveness in the older population ii. Down-regulation of influenza virus genes with novel sirna-chimeric-ribozyme constructs
Madhu Khanna, University of Delhi, India
Title : Commensal bacteria drive B-cell lymphomagenesis in the setting of innate immunodeficiency
Ping Xie, Rutgers University, United States
Title : The role of immunity in the pathogenesis of SARS-COV-2 and in the protection generated by COVID-19 in different age groups
Ahmed Abdulazeez, BHRUT Trust, United Kingdom
Title : Establishing a platform method for physical appearance assessment of new parenteral pharmaceuticals
Ying Wan, Merck & Co., United States
Title : Evaluating the immunogenic impact of process impurities in mRNA vaccine production: Establishing integrated control strategies and specifications
Jesse Kuiper, Merck Research Laboratories, United States
Title : New biomarkers in leishmania major vaccine development
Negar Seyed, Pasteur Institute of Iran, Iran (Islamic Republic of)
Title : Advances in vaccines: Revolutionizing disease prevention
Delia Teresa Sponza, Dokuz Eylul University, Turkey