ComplianceOnline

Detection of PCV1 Virus Caused Temporary Suspension of Rotarix Vaccine

  • Date: March 22, 2010
  • Source: Admin
Webinar All Access Pass Subscription Abstract:

FDA is requiring the healthcare practitioners to temporarily stop using Rotarix vaccine, manufactured by GlaxoSmithKline (GSK) for rotavirus immunization in the US, as the FDA wishes to learn more about components of a superfluous virus detected in the vaccine. However, there is no evidence at this time that this finding poses a safety risk.


 

Bookmark and Share

Trending Compliance Trainings

HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms
By - Roger Cowan
On Demand Access Anytime
Extractables and Leachables in Early Phase Development
By - Wayland Rushing
On Demand Access Anytime
CGMP controlled Raw Materials
By - Charity Ogunsanya
On Demand Access Anytime
OTC Drug Regulations
By - Loren Gelber
On Demand Access Anytime
Veterinary Feed Directive (VFD) Final Rule - What you need to know
By - Bernadette Alisantosa
On Demand Access Anytime
Best Sellers
You Recently Viewed
    Loading