Isolators and RABS Technology for Pharmaceuticals Aseptic Processing
Restricted Access Barrier Systems (RABS) are intermediate technology between traditional cleanrooms and full isolators....
Pharmaceuticals Sterile Dosage Forms and Aseptic Processing
Sterile products can be manufactured by two primary methods: 1) Terminal sterilization (product sterilized in final...
Pharmaceuticals Solid Dosage Manufacturing Facility Design
Solid dosage forms, primarily tablets and capsules, represent the largest category of pharmaceutical products by...
PIC/S Classification System for Pharmaceutical Sterile Products
The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S) is an international...
ISO Cleanroom Classification System in Pharmaceuticals
According to ISO 14644-1, a cleanroom is "a room in which the concentration of airborne particles is controlled,...
Cleanroom Classification and Design - Details
Cleanrooms are specially designed and maintained environments where the concentration of airborne particles is...
Cleanrooms and GMP Design of Pharmaceutical Facilities
Cleanrooms provide controlled environments where airborne particulate contamination is limited to levels appropriate...
Bill of Materials (BOM) Number in Pharmaceuticals
A BOM (Bill of Materials) number serves as a unique identifier for a specific set of materials associated with a Master...
Pharmaceuticals Manufacturing Process (Tablet Compression)
A Quality by Design (QbD) approach to understanding tablet compression failures and preventing them through proper...
