The document discusses Good Laboratory Practices (GLP) for pharmaceutical quality control laboratories. It covers GLP requirements from regulatory authorities like the FDA and WHO. The presentation is divided into sections on lab management, resource management, and quality control activities. Lab management covers topics like laboratory entry and exit procedures, safety, and upkeep. Resource management addresses management of personnel, procedures, reagents, instruments, and documentation. Quality control activities include sampling, chromatography, microbiology, stability testing, and documentation of investigations. Maintaining GLP standards helps ensure quality products for patients and regulatory compliance.
2. The IBN SINA Pharmaceutical Industry Ltd. is
committed to
Serve humanity by manufacturing and providing quality medicines and
services to its customers ;
Maintaining the ethical standard in all its functions following the
requirements of cGMP and regulatory authorities ;
Marching onward for sustainable growth and continual improvement.
69. Thank You
Thank you for attending this training course.
By keeping the data quality attributes (ALCOA) in the forefront of our minds,
we can:
Supply safe and effective products to our patients and consumers
Maintain compliance so that we can .
Keep in mind that the customers and patients relies on us and
the accuracy of our data!