TEST METHOD FOR AIR CHANGE RATE (ACR) IN ASEPTIC DISPENSING FACILITIES
Introduction:- Conventional clean rooms operate on the principle that the air supplied to the room is of sufficient quantity to dilute or remove the contamination…
Category: Pharma Manufacturing
CLEANING VALIDATION ACCEPTANCE LIMITS FOR PHARMA MANUFACTURING OPERATIONS
DETERMINATION OF CLEANING VALIDATION ACCEPTANCE LIMITS FOR PHARMACEUTICAL MANUFACTURING OPERATIONS Residue Limits:- Validating a cleaning process includes selecting target residues and setting limits for those…
TABLET COMPRESSION: MACHINE DESIGN
Press Design and Layout:- Modern rotary tablet presses are typically designed in separate machine sections (press zones). Typical sections to provide separation and isolation of…
TABLET COATING AND ITS DIFFERENT METHODS
INTRODUCTION:- Tablet is a pharmaceutical solid dosage form, comprising a mixture of active substances and excipients, commonly in powder form, pressed or compacted right into…
PACKAGING OF PHARMACEUTICAL DOSAGE FORMS
INTRODUCTION:- Packaging is the process by which the pharmaceuticals are suitably placed so that they should retain their therapeutic effectiveness from the time of their…
PERSONNEL TRAINING FOR PHARMACEUTICAL INDUSTRY 2
INTRODUCTION:- The pharmaceutical industry is facing a tremendous changes and challenges nowadays. It has been observed that lack of proficient, talented, capable employees has enforced…
PERSONNEL TRAINING FOR PHARMACEUTICAL INDUSTRY 1
INTRODUCTION: – The pharmaceutical industry is facing a tremendous changes and challenges nowadays. It has been observed that lack of proficient, talented, capable employees has…
DIFFERENT TYPES OF CLEANING METHODS USED IN PHARMA
CLEAN-IN-PLACE: – Cleaning applications can be classified into two groups based on the extent of disassembly-CIP (clean-in-place) and COP (clean-out-of-place). Technically, CIP applies to all…
SELF INSPECTION OF PREMISES
A systematic inspection program to detect any shortcomings in the implementation of cGMP and to recommend necessary corrective actions. Manager QA/Head QA shall nominate the…
5S IN PHARMA INDUSTRY
A process industry is commonly referred to as a manufacturing process where a chemical change has taken place, and it includes segments such as glass…
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