What are the Key Components of GMP in Cancer Drug Manufacturing?
The key components of GMP in cancer drug manufacturing include:
Raw Material Quality: Ensuring that all materials used are of high quality and free from contamination. Facility Design: Designing facilities that minimize contamination risks and allow for easy cleaning and maintenance. Environmental Monitoring: Regular monitoring of the production environment to ensure it meets cleanliness standards. Batch Records: Keeping detailed records of each production batch to trace any issues back to their source. Sterility Testing: Ensuring that sterile products are free from microbial contamination.
