Cleaning Validation – Qvents

Qvents

Discussion forum for Pharma Quality events, Regulatory Actions

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

2 minutes read Uncategorized

Updated on September 20, 2024

Updated on September 20, 2024

APIC (Active Pharmaceutical Ingredients Committee): Guidance On Aspects Of Cleaning Validation In Active Pharmaceutical Ingredient Plants
European Medicines Agency (EMA): Guideline on setting health based exposure limits; Questions and answers on Guideline on setting health-based exposure limits
EMA: Questions and answers on implementation of risk-based prevention of cross-contamination in production and ‘Guideline on setting health-based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities’ (EMA/CHMP/CVMP/SWP/169430/2012)
USFDA Guide To Inspections : Validation Of Cleaning Processes
PIC/S: Guideline On Setting Health Based Exposure Limits For Use In Risk Identification In The Manufacture Of Different Medicinal Products In Shared Facilities (PI 046-1 Annex 1 July 2018)
PICS::Questions and Answers on Implementation of Risk-Based Prevention of crosscontamination in Production and ‘Guideline on setting Health-Based Exposure Limits for use in risk identification in the manufacture of different medicinal products in shared facilities
PICS::AIDE-MEMOIRE Inspection of Health Based Exposure limit (HBEL) assessments and use in Quality Risk Management
TGA: Cleaning Validation – A regulatory perspective (Presentation)
WHO TRS 1033 – Annex 2: Points to consider when including Health-Based Exposure Limits (HBELs) in cleaning validation
Useful Info: Agency Expectations on PDE Determination and PDE Reports; GMP Verlag: LOGFILE Feature 14/2024

Share: