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Subscribe NewsletterGMP Auditor Training for Pharmaceutical Companies
Product Id
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600115
Overview: Because of the extreme criticality of GMP audits and the potential consequences, many pharmaceutical manufacturers have adopted a program of internal GMP audits in order to find and correct areas where the firm is not in full compliance with the GMP regul
By identifying areas of non-compliance, firms have an opportunity to correct the situation before an FDA audit occurs. There are several problems with this approach, however. The auditors may not fully understand the regulations and may not have been trained in audit techniques. Another impediment is that an internal auditor is monitoring his/her friends. It is very difficult to point out errors committed by a friend since by calling attention to a lack of compliance may be interpreted as "telling on" the friend and possibly causing a problem for them.
This program will cover two major topics. First, we will discuss auditing. This portion will show what an auditor does and how an audit is conducted We will also stress the difficulties faced by an auditor who is from within the organization being audited. The second portion of this program will present an overview of the various GMP regulations that a manufacturer must work within. Lastly, we will identify the most commonly cited GMP violations and show how they are found and identified. Topics included in this presentation include:
By identifying areas of non-compliance, firms have an opportunity to correct the situation before an FDA audit occurs. There are several problems with this approach, however. The auditors may not fully understand the regulations and may not have been trained in audit techniques. Another impediment is that an internal auditor is monitoring his/her friends. It is very difficult to point out errors committed by a friend since by calling attention to a lack of compliance may be interpreted as "telling on" the friend and possibly causing a problem for them.
This program will cover two major topics. First, we will discuss auditing. This portion will show what an auditor does and how an audit is conducted We will also stress the difficulties faced by an auditor who is from within the organization being audited. The second portion of this program will present an overview of the various GMP regulations that a manufacturer must work within. Lastly, we will identify the most commonly cited GMP violations and show how they are found and identified. Topics included in this presentation include:
- Audit techniques
- Time requirement for a full audit
- Origin of GMP regulations
- GMPs to be monitored during an internal audit
- Most common FDA citations for non-compliance
Why should you attend:
Regular audits of vendors are not only required by US law, it is good business. Vendors tend to make changes in their manufacturing process that can unknowingly affect the quality of the product being manufactured. While the vendor's motivation may be harmless, the impact on the unsuspecting customer may be significant. Since the vendor will not tell his customers of the change, the only way to learn of these changes is a vendor audit. Another important use of GMP audits is to self-inspect your own manufacturing facilities to find practices that might result in FD 483 citations in the next inspection of your facility.
Areas Covered in the Session:
- Why audits are conducted
- How to conduct an audit
- What to look for
- Common citations in facilities
- Common citations for documentation
- Auditing of records
- Organizational citations
- Laboratory audits
- Validation
Who Will Benefit:
- Supervisors
- Managers
- Directors
- VPs of Manufacturing or Quality