Devine Guidance

MHLW MO 169 – Chapter 2/Section 6 – Internal Audit

Ohayou Gozaimasu. This week the term/phrase specific to Japan, the doctor would like to introduce to the readers, is “CJO wo sagashite imasu” or for those of you with some degree of literacy in Japanese “CJO を探しています。” The literal translation is “I am looking for the CJO (Chief Jailable Officer).” If a regulatory body comes looking specifically for the CJO, and you are the CJO, you just might want to consider lawyering up.

In this edition of Devine Guidance, the doctor will explore the need for performing internal audits. The doctor would like to add that the performance of timely audits or in some cases, not performing audits at all is one of the frequent non-conformances cited by Dr. D during the performance of audits for my clients. True story, I visited a supplier earlier in the year that emphatically stated that their organization “really did not have to actually perform audits, just plan for them.” Do you know how difficult it was for the doctor to keep from laughing hysterically? But hey, audits are a learning experience and hopefully the lesson taught by Dr. D was a memorable one.  

Internal audits, regardless of the regulatory environment, are a fundamental requirement for an effective QMS. ISO 13485:2012; 21 CFR, Part 820, and Ministerial Ordinance 169 (MO 169), each clearly specifies that device manufacturers must plan and perform internal quality audits in order to gauge the overall effectiveness of the QMS. That being said, I hope you enjoy this week’s guidance.

 

The performance of an effective internal audit is a mission-critical requirement that organizations use to gage the effectiveness of their QMS and drive overall organizational improvements. MO 169’s requirement for internal audits contains sufficient granularity (similar to ISO 13485) for a device manufacturer to implement an internal audit program. The requirements for the internal audit program are relatively straight-forward. The internal audit program must: 

• Be documented by an established procedure;
• Ensure audits, assessing all aspects of the QMS, are performed;
• Define audit frequency;
• Define the publishing of an audit schedule;
• Define audit scope and methods employed for auditing;
• Contain requirements and skills for auditors (recommend reading ISO 19011);
• Contain a requirement that auditors cannot audit their own work or functional organization;
• Ensure audit results, including non-conformances noted, are recorded and retained as a quality record;
• Ensure re-audits and increased frequency of audits are performed for problem areas; and
• Ensure that corrective action is pursued when non-conformances are identified during the execution of an internal audit.

Dr. D appreciates the manpower resource challenges facing medical device manufacturers, especially small and medium size device manufacturers. The good news is hiring Second Party Auditors (a.k.a. consultants like Dr. D) is an acceptable practice. The key is to ensure the Second Party Auditor is competent.

Another point Dr. D would like to make is that if your organization decides to use an external auditor, make sure the auditor trains to your Internal Audit SOP and evidence of this training is documented. 

From the doctor’s stand point there are a number of different ways to meet the internal audit requirement. One – break the schedule down into small bites and spread the audits out monthly, covering the course of the year. Two – break the audits down into quarters and execute audits four times a year. Three – perform at least a well-scripted annual audit (least preferred approach). Regardless of the path, pick one, document it, and execute the audit(s). Please do not be that organization that states audits just have to be planned. Before the doctor forgets, it is always considered a best practice to map your organization’s QMS to specific regulatory requirements. That being said, Table 1.0 reflects an approach for mapping an Internal Audit requirement.  

Table 1.0 – Sample Requirements Matrix
Procedure	Procedure Name	Requirement	21 CFR, Part 820	EN ISO 13485:2003	MHLW MO 169
1266-1 Rev B	Internal Quality Audits	Internal Audit	820.22	8.2.2	Article 56

 

For this edition of DG, the doctor will leave the readers with four takeaways.

• Use the internal audit program to gage the effectiveness of the QMS and to drive continuous improvements.
• Performing internal audits is not optional. Internal audits are mandated by MO 169.
• Make sure internal auditors are adequately trained (reference ISO 19011).
• If your organization does not have the resources available to perform internal audits, it is an acceptable practice to hire a 2nd Party Auditor (give Dr. D a Call).

Until the next edition of DG, when the doctor provides guidance on MO 169 – Chapter 2, Section 6 “Measurement, Analysis, and Improvement” (Articles 57 through 59 Measuring and Monitoring of processes, Products, and Specialty Devices), sayonara from Dr. D and best wishes for continued professional success.

References: 

1. Code of Federal Regulation. (2011, April). Title 21 Part 820: Quality system regulation. Washington, D.C.: U. S. Government Printing Office.
2. EN ISO 13485:2012. (2012, February). Medical devices – quality management systems – requirements for regulatory purposes (EN ISO 13485:2012).
3. Linguanaut the Japanese phrases and expressions. (2012). Retrieved September 8, 2012, from http://www.linguanaut.com/english_japanese.htm
4. Ministerial Ordinance 169. (2004). MHLW ministerial ordinance 169 on standards for manufacturing control and quality control for medical devices and in-vitro diagnostic reagents. Retrieved June 1, 2012, from http://www.pmda.go.jp/english/service/pdf/ministerial/050909betsu3.pdf