ISPE CEUs: 1.3
Type: Classroom Training Course
Auditing is a critical function within a pharmaceutical company. It provides management with information about how effectively the company controls the quality of their processes and products. Auditors must perform their jobs competently to ensure their company’s compliance with pharmaceutical USFDA GMP regulations and other quality standards like ICH Q10. Auditing for GMP is specifically designed to address the challenges of GMP auditing for the pharmaceutical industry and present the basic competencies required to effectively perform the auditor's assigned responsibilities and contribute to the improvement of auditor performance within a regulated industry.
Note: This course is not designed to prepare companies to be audited and does not contain content for medical device auditing.
For Medical Device Auditing, please refer to the ISPE online Training Auditing for Medical Devices.
This training course is of particular interest to existing and future members of the ISPE Process/Product Development (COP).
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|13 Mar 2017 -
14 Mar 2017
|Tampa, FL USA||
|06 Nov 2017 -
07 Nov 2017
|Tampa, FL USA||
To qualify, all registrant information must be submitted at the same time; only ONE payment to cover all registrations will be accepted. Registrations that arrive later will NOT be eligible for the group discount. Cannot be combined with other offers. To register as a group, please contact ISPE by telephone, +1-813-960-2105.
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This course can be offered at your company site in its current format or customized to meet the needs of your organization.