LEAK TESTING OF AEROSOLS
All filled aerosol cans are leak tested before distribution to prevent an empty or near-empty product from reaching the patient. Four methods are currently used…
Category: Pharma Industry Guidelines
SOP FOR MICROBIAL LIMIT TEST FOR THE ESTIMATION VIABLE AEROBIC MICRO-ORGANISMS
1.0 OBJECTIVE : To laid down procedure for microbial limit test in for the estimation of the number of viable aerobic micro-organisms present and for…
SOP FOR OPERATION AND CALIBRATION OF DIGITAL AUTOMATIC KARL FISCHER TITRATOR
1.0 OBJECTIVE : This procedure is laid down to explain the mode of operation & calibration of Digital Automatic Karl Fischer Titrator. (Make: VEEGO, MODEL…
SOP FOR OPERATION OF TOTAL ORGANIC CARBON ANALYSER 1
1.0 OBJECTIVE : To laid down the procedure for operation of Total Organic Carbon Analyser (Sievers-900). 2.0 SCOPE : This procedure is applicable to…
QUALITY CONTROL OF PACKAGING MATERIALS
INTRODUCTION: – In pharmaceutical industry it is vital that package selected preserve the integrity of product. The selection of package begins with determination of products…
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…
ENVIRONMENT MONITORING BY SETTLE PLATES IN ASEPTIC FACILITY
Introduction:- Settle plate sampling is a direct method of assessing the likely number of microorganisms depositing onto the product or surface in a given time.…
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…
TYPES OF MICROBIOLOGICAL SAFETY CABINETS (MSCS)
Class I:- A cabinet with a front aperture through which the operator can carry out manipulations inside the cabinet. This type of cabinet is suitable…
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