- SRF Limited -Walk-In Interviews for Production, Instrumentation, Electrical & Polymer Process On 20th & 21st May’ 2022
- Biocontamination control techniques in Purified Water System
- SOP on Monitoring of Compressed air and Nitrogen for Microbial analysis
- SOP on Sampling and testing procedure of swab sample
- SOP on Preservative Efficacy Test of Oral Preparations
- SOP on Monitoring of Bioburden of Packing material
- SOP on Operation, Cleaning and Maintenance of Microscope
- SOP on Cleaning of Glass ware for Microbiology
- Performance Qualification – LAF (Laminar Air Flow)
- Disinfectant Validation Procedure
- Calibration of steam sterilizer (Autoclave)
- Negative Control & Positive Control in Microbiological Sterility Testing.
- Qualification of Nitrogen Gas Producing System-for Sterile Manufacturing
- Motility by Hanging Drop Method
- UV Light Validation
- Spore Staining – A Basic Overview
- Identification of Location for Settle Plate Exposure in Pharmaceutical Mfg. Area
- SOP on Operation, Calibration, Cleaning and Maintenance of BOD Incubator
- SOP on Operation, Calibration, Cleaning and Maintenance of M Air T Air Sampler
- SOP on operation, cleaning and maintenance of Fogger and Fogging of Microbiology Testing Areas
- SOP on Motility test by Hanging drop Method
- SOP on General Safety in Microbiology Laboratory
- SOP on Spore Staining
- SOP on Cleaning and Disinfection of microbiology lab
- SOP on Entry and Exit procedure for Microbiology Laboratory
- SOP on Receipt, Issuance, storage, Stock maintenance & Preparation of Media
- Microbial Limit Test (MLT)…Basic Approach in pharmaceuticals..!!!
- bacterial endotoxin tests
- Overlook on VIRUSES….!!!
- SOP on Product Bioburden Testing
- Growth Promotion, Inhibition, Sterility and Indicative Test and its Acceptance Criteria
- Qualitative, Quantitative and Semi-quantitative Testing in Microbiology
- Usage of BOD & Bacteriological Incubator & their Differences
- Ultra Violet Light – Role & Application in Pharmaceuticals
- Why reused glasswares are sterilized by air dry heat method for parenteral lab testing
- Health Risk factors of Formaldehyde as comman fumigation (why banned)
- Identification of Sampling Location for settle plate method during bio load montoring of Production Area
- All Endotoxins are Pyrogens but all Pyrogens are not Endotoxins
- Bacterial Endotoxin Test (BET)
- The Use of Risk Assessment Tools For Microbiological Assessment of Cleanroom Environments
- Revision of the General Chapter on Pharmaceutical Water in the US Pharmacopoeia
- WHO Defines Requirements on Zones E and F
- What are Selective, Differential, Enriched, Nutrient and Minimal Media?
- Fact Sheet: Environmental Monitoring and Control
- Is Fungal Count Acceptable in Pharmaceutical Classified Area?
- Selection of Incubation Conditions for Environment Monitoring Plates in Pharmaceutical Microbiology
- Why Incubator is Called BOD Incubator?
- Vacuum Leak Test (VLT), Acceptance Criteria and its Importance in Pharmaceuticals
- What is the Difference Between BOD and Bacteriological Incubator?
- How to Select Sampling Locations for Environment Monitoring Programme?
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