The top generic drug regulator at the US Food and Drug Administration (FDA) on Wednesday touted the drop in refuse-to-receive ...
The US Food and Drug Administration (FDA) has issued warning letters to several drug manufacturers and compounders for ...
The European Association of Medical devices Notified Bodies (Team-NB) is concerned that some of the targeted revisions ...
The US Food and Drug Administration (FDA) has issued warning letters to several drug manufacturers and compounders for violations of current good manufacturing practices (CGMP) and for marketing ...
The US Food and Drug Administration (FDA) has released a draft guidance document aimed at setting impurity limits for ...
The European Association of Medical devices Notified Bodies (Team-NB) is concerned that some of the targeted revisions ...
The National Medical Products Administration (NMPA) has published rules strengthening the supervision and administration of ...
The new member-exclusive RAPS Journal of Regulatory Affairs, a bimonthly, peer-reviewed publication building on the success ...
RAPS Collaborative Communities bring together regulatory professionals who share common interests, specialties, and challenges. These member-only topic-based forums create space for meaningful ...
The US Food and Drug Administration (FDA) has issued a warning letter to Purolea Cosmetics Lab for several violations of Good ...
Welcome to another installment of This Week at FDA, your weekly source for updates – big and small – on FDA, drug and medical ...
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