Control of impurities in drug substances and drug products is very critical in assuring their quality. Types of impurities in finished product on its manufacturing process more so for drug substances.
The lecture covers implementing a cleaning validation program based on risk approach. Higher the risk, more rigorous should be the cleaning procedure and should be validated.
Validation of pharmaceutical manufacturing processes is a very important element of GMP in order to provide high level of confidence on the quality of finished product and is a mandatory compliance requirement of FDA.
This session will provide examples and techniques to deal with different type of auditees & audits, that are not taught during the traditional auditor certification training.
This session will provide examples and techniques to deal with different type of auditees & audits, that are not taught during the traditional auditor certification training.
This live webinar is intended to provide attendees with information on implementing purchasing policies for purchasing professionals. Attendees should leave the program with practical applications that they can apply to their daily business.
Behavioural issues and conflict in the workplace are inevitable. Whenever you have diverse groups of people working together on a daily basis, conflict will arise.