Qvents

Qvents

Discussion forum for Pharma Quality events, Regulatory Actions

Warning letters, 483s, Recalls, Import Alerts, Audit observations

Facility Registration Violations, Refusa

Indian API manufacturer Jagsonpal Pharmaceuticals was issued a Warning Letter by the US FDA in

Delaying, Denying, Limiting, Refusing In

Chinese OTC Manufacturer Tianjin Darentang Jingwanhong Pharmaceutical Co., Ltd was inspected by USFDA in March

FDA Final Guidance: Delaying, Denying, L

FDA has issued final guidance on Circumstances that constitute Delaying, Denying, Limiting, or Refusing a

Members of US Congress writes to FDA:Rai

The letter to FDA was written by the Republican members of the E&C committee of

Industry will see more unannounced inspe

In an Interview to CNBCTV18 during visit to India, USFDA Commissioner touched on different topics