1.0 OBJECTIVE: To lay down a procedure for Energy Review 2.0 SCOPE: This SOP is applicable to Energy management System. 3.0 RESPONSIBILITY: 1. Electrical Maintenance Department is responsible for measurement of electrical energy consumption at each location. 2. Concerned HOD is responsible for recording ...

1.0 OBJECTIVE: To lay down a procedure for shutdown of area or system or equipment. 2.0 SCOPE: This SOP is applicable for shut down work to be carried out. 3.0 RESPONSIBILITY: Concern User Department : Department Manager –Intimation to all sections QA : Review and approval for execution 4.0 ACCOUNTABILITY: ...

1.0 OBJECTIVE: To lay down a procedure for handling of primary standard. 2.0 SCOPE: This SOP is applicable to handling of primary standard used for standardisation of volumetric solution and calibration purpose in quality control department. 3.0 RESPONSIBILITY: Officer, Executive – Quality control Head ...

Microbiological contamination control is the process of preventing the introduction of infectious materials like bacteria, yeast, mold, fungi, viruses, prions, and protozoa. The three standard options for contamination control are prevention, cleaning, and monitoring. Reduce Contamination in a lab ▪️Wear ...

Sterility testing is a microbiology laboratory test that assesses if a product is free of viable microorganisms, or sterile. It’s performed on manufactured biological materials, such as blood products, pharmaceutical products, and sterile medical devices. The industry standard for sterility testing ...

The most common bacteria found in environmental waters are E. durans, E. faecalis, E. faecium, and E. hirae. Other common bacteria include E. avium and E. cecorum. Bacteria that can be found in drinking water include Coliform Bacteria A group of bacteria that can be found in soil, plants, and the digestive ...

Pharmaceutical industry, water purification systems typically involve multiple stages to ensure high-quality purified water. A multimedia filter is a water filtration process that uses multiple layers of media to pass water through. The layers are progressively sized in coarseness and depth, with the ...

Sterility testing is a microbiology laboratory test that assesses if a product is free of viable microorganisms, or sterile. It’s performed on manufactured biological materials, such as blood products, pharmaceutical products, and sterile medical devices. The industry standard for sterility testing ...

Cleaning validation establishes that the cleaning procedure can effectively remove product residue from pharmaceutical equipment to an acceptable limit. Cleaning validation is a critical step in the pharmaceutical manufacturing process that ensures the safety of patients by preventing cross-contamination ...

Microbiological test that evaluates the ability of aseptic manufacturing personnel to prevent contamination during drug production. The test uses a sterile microbiological growth medium, such as Triptic Soy Broth (TSB), to assess the technique and competency of personnel to perform tasks such as filling, ...