Discussion forum for Pharma Quality events, Regulatory Actions
Warning letters, 483s, Recalls, Import Alerts, Audit observations
Warning letters, 483s, Recalls, Import Alerts, Audit observations
Forums is a platform where you can raise queries and discussions on Pharma GMP / Regulatory / Technical issues. Other users can see your query and can respond. Please post your queries with a brief Topic, Title and Description of the query (describe your query /problem).
The Forum page is structured as main Forums, Subforums and Topics. Under each main Forum there are Subforums and under each Subforums there are different Topics. You can navigate to an existing Topic under a Subforum and participate in the discussion (reply / comment) or add a new Topic title under a Subforum and describe your query.
If you are not able to find an appropriate Forum/Subforum, Post your Query under Others (Qvents team will categorise the query into appropriate Forum/Subforum or create new Forum)
