Good Laboratory Practices (GLP) play a crucial role in ensuring the integrity, reliability, and ethical conduct of nonclinical safety studies. Let’s delve into why companies emphasize GLP compliance: 1. Regulatory Requirements: GLP regulations provide a standardized framework for conducting nonclinical studies in drug development. Regulatory agencies, such as the FDA and EMA, mandate…
1. Test facility, organization and personnel 2. Quality Assurance (QA) program 3. Facilities 4. Apparatus materials and reagents 5. Test systems – Appropriate design and adequate capacity of apparatus used for the generation of data – Integrity of physical/chemical test systems – Proper conditions for storage, housing, handling and care –…
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. Contamination Control in Lab To Avoid Contamination in Microbiology Lab By implementing these practices consistently, microbiology labs…
GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice) are both quality assurance systems that are crucial in the pharmaceutical manufacturing industry. While they share some similarities, there are also notable differences between the two concepts. Standards: 1. GMP: GMP focuses on ensuring that pharmaceutical products are consistently produced and controlled according to quality…
1. Always wear appropriate personal protective equipment (PPE) such as gloves, lab coat, and safety goggles. 2. Familiarize yourself with the laboratory’s emergency procedures and know the location of safety equipment like fire extinguishers and eyewash stations. 3. Keep your work area clean and organized to prevent accidents and cross-contamination. 4. Label all containers clearly…
