On-line Advance Training Session
In 2004 APIs were defined as the critical raw materials to be audited. Do we really audit the GMP compliance, or we just believe their speech? Is that a critical activity or a commodity?
In this on-line course, the real GMP auditing criteria for API manufacturing will be reviewed.The following topics will be covered:
The manufacturing and control of these products are subject to Good Manufacturing Practice (GMP) to ascertain the quality and safety for the patient and to obtain reliable and integer data to support its qualification.
Examples of most common observations will be shown during the course, and it will be enabled a space for questions and answers.
Professionals opearting in the Pharmceutical business wishing to improve their resources and knwoledge on performing effective supplier audits.