Clinical Trials and Regulatory Affairs

Clinical trials and regulatory affairs are critical components in the development and approval of vaccines, ensuring that they are both safe and effective for public use. Clinical trials follow a rigorous, multi-phase process to evaluate a vaccine's efficacy, safety, and optimal dosage, involving diverse participant groups to assess its impact across different populations. Each phase of the trial provides valuable data, from initial safety assessments in small groups to broader efficacy studies in larger populations. 

 

    Related Conference of Clinical Trials and Regulatory Affairs

    February 27-28, 2025

    8th International Conference on Vaccines and Immunology

    Paris, France
    April 28-29, 2025

    2nd Global Summit on Vaccines & Emerging Diseases

    Bali, Indonesia
    July 28-29, 2025

    43rd Euro Global Summit and Expo on Vaccines & Vaccination

    Aix-en-Provence, France
    September 18-19, 2025

    7th World Congress on Vaccine and Immunology

    Amsterdam, Netherlands

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