Qvents

Qvents

Discussion forum for Pharma Quality events, Regulatory Actions

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

WHO Publishes Comprehensive Guidelines f

WHO has published a comprehensive and easy to understand guideline for control of nitrosamines in

CDSCO Notifies New Online Export NOC Sys

Indian drug regulatory, CDSCO has notified the new online Export NOC system for Unapproved Drugs

Timeline for Revised Schedule M Implemen

Health Ministry in India has extended the timeline for implementation of the revised Schedule M

FDA Issues New Guidance on 21 CFR 211.11

The FDA has issued new guidance on “Considerations for Complying With 21 CFR 211.110.” According

Delaying, Denying, Limiting, Refusing In

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

New FDA Guidance: Review of DMFs in Adva

The USFDA has published a new guidance titled “Review of Drug Master Files in Advance

FDA Updates Guideline for Control of Nit

FDA has issued an Updated Guidance for Control of Nitrosamines in Human Drugs in September

FDA Final Guidance: Delaying, Denying, L

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

CEP for Sterile Drug Substances: EDQM is

EDQM has published the draft guideline on Content of the dossier for sterile substances for

FDA issues Guidance on Facility Readines

The guidance provides information on how FDA decides goal dates for a drug application (ANDA,