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Viral VectorProcess Development explained

Viral Vector process development explained – from Upstream to Downstream

...Guidelines relevant for advanced therapy medicinal products. https://www.ema.europa.eu/en/human-regulatory/research-development/advanced-therapies/guidelines-relevant-advanced-therapy-medicinal-products Cellular & Gene Therapy Guidances. https://www.fda.gov/vaccines-blood-biologics/biologics-guidances/cellular-gene-therapy-guidances EudraLex The Rules Governing Medicinal Products in the European Union, Volume 4 Good Manufacturing Practice. https://ec.europa.eu/health/sites/health/files/files/eudralex/vol-4/2017_11_22_guidelines_gmp_for_atmps.pdf...

About us

...the most suitable path and to guide you through your clinical journey. We can make your CMC-journey easier. https://www.youtube.com/watch?v=lvGsMkNUjrE Why do clients choose Biovian as a CDMO partner – Video...
Greetings from the CEO of Biovian

Video Greetings from the CEO of Biovian

...we have experienced a lot of positive developments at Biovian that I want to share with you“. He also takes a look at the opportunities for growth in 2021. https://www.youtube.com/watch?v=pvkgGlrEYfY...
Biovian in GEN magazine. 360-Degree View of AAV Production

Biovian in GEN Magazine – A 360-Degree View of AAV Production

...systemic delivery over local administration and study larger patient populations. Different applications require vastly different amounts of vector. We need to have something to adjust for that massive difference.  https://www.genengnews.com/sponsored/a-360-degree-view-of-aav-production/...

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Download a brochure Thank you! Your download is ready. Stay up-to-date with our latest news and events Follow us on Contact https://youtu.be/PWt6mtUYNAI Viral Vector and recombinant protein CDMO – Video...