The Master Formula Record (MFR) and Bill of Material (BOM) are essential documents in the pharmaceutical industry, providing comprehensive details for the formulation and manufacturing of pharmaceutical products. The MFR…
Compressed air validation is recorded evidence that such parameters as aerosol particle content, dew point, liquid water concentration, vapor content, oil aerosols, and other pollutants are within limits and do…
d Standard Operating Procedure (SOP) for Bacterial Endotoxin (LAL) Test in microbiology for pharmaceutical and healthcare laboratories and food industry. With our comprehensive Bacterial Endotoxin (LAL) Test Procedure, you may…