In Infectious disease research, early-phase development is moving fast. To keep up, leading teams are rethinking how they work, from improving sample stabilization and enabling outpatient models to generating high-quality, regulatory-ready data from day one.

This eBook from hVIVO explores practical ways to make your programs leaner, more predictable, and scientifically stronger, right from the start.
Why this eBook matters
In vaccine and antiviral development, small operational improvements can lead to significant timeline gains. Forward-thinking teams are optimizing early-phase research to drive faster, more confident progress.
Discover how modern teams are:
- Strengthening early-phase study design
- Improving sample handling and stability strategies
- Streamlining outpatient and clinical workflows
- Generating regulator-relevant data earlier
- Reducing downstream programme risk
- Aligning with regulatory expectations from the start

About hVIVO
hVIVO is a full-service early phase CRO offering end-to-end drug development services from preclinical consultancy through to Phase III clinical trials, including world leading end-to-end human challenge trials services. With decades of experience in rapidly delivering data for our global client base, our team brings together strategic insight and operational expertise to deliver a variety of clinical study types across multiple locations.
To support rapid study start-up and reliable delivery, our dedicated recruitment teams in Germany and the UK provide direct access to both healthy volunteers and patient populations. This is complemented by our integrated drug development consultancy as well as our infectious disease and immunology laboratories and biobanking services.
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