Internal Auditing to MDSAP: Concepts and Practices

Date: Jan 17, 2024

Time: 1 PM EST

Duration: 60 Minutes

Level: Intermediate to Advanced

Group Packages: Please contact ben@complyrules.com

Description

This course will give an introduction into the Medical Device Single Audit Program (MDSAP) and how to adjust your internal audit program. The introduction will give an overview about the requirements for the quality management system and how to conduct an internal audit with MDSAP requirements to check, if your quality management system meet all MDSAP requirements.

Why Should You Attend:

You should attend this webinar to understand, what how is MDSAP working in relation to your internal audit program and how to adjust your internal audit program and finally how to conduct an internal audit according MDSAP requirements.

This webinar will give you a clear structured overview and introduction, how to apply MDSAP-Requirements in your internal audit program and to conduct internal audits with MDSAP requirements. First you learn to identify the relevant requirements, second you learn how to implement the identified requirements into your audit program. The course based on the MDSAP Companion-Document, issued by the FDA.

Areas Covered in the Webinar:

• What is the Medical Device Single Audit Program (MDSAP)?
• Which Companies must have MDSAP?
• Which Companies should have MDSAP?
• How to setup and audit program under MDSAP?
• How to conduct an audit under MDSAP?
• How the MDSAP-Audit is working?

Frequently Asked Questions:

1. Can ORA perform a surveillance inspection of a combination product at a firm participating in the Medical Device Single Audit Program (MDSAP)?
2. How will MDSAP ensure that every RA has the same evaluation standards for the Auditing Organization?
3. How do I find out more specific information on the documents, policies, and procedures used in the MDSAP?
4. Can industry provide input into MDSAP documents or the program in general?
5. What is the best way to determine what is expected of the Auditing Organizations with regard to multiple jurisdictions?
6. Can Contract Research Organizations participate in MDSAP and What about Certified Quality Auditors?
7. If an RA decides to change its GMP/QMS or Regulatory requirements, how will the changes be incorporated into MDSAP?
8. Can an Auditing Organization contest an unfavorable recognition decision or a nonconformity and its grading?
9. How do Auditing Organizations ensure that duplicate efforts are not performed during an audit of a manufacturer that sells in multiple jurisdictions?
10. How are nonconformities that are identified during an MDSAP audit managed? What is the timeline for a manufacturer to respond to nonconformities?
11. Where you mentioned outsourced processes are typically not audited via MDSAP, could we anticipate that there is a higher chance that the FDA could choose to perform an inspection of a contract manufacturer?
12. Is the estimated durations what is recommended for internal audits as well as 3rd party?
13. Would it be required to use the MDSAP grading of nonconformities when conducting the internal audit?
14. Is a root cause analysis needed regardless of the finding grade?
15. Can you please highlight country specific requirements?
16. No. if there is a finding grade 5, understandably a root cause analysis is needed. What if it is a finding grade 1, not as severe?
17. I understand the grading. Indirect not repeat without device on the market means 1 and it is typically not high risk.
18. Where in the MDSAP documents is "repeat" defined? Is the assumption just the next time audited?
19. Is "repeat" the second NC within the direct or indirect sections or the next time we are audited?
20. Question came up during an internal audit - how to show compliance with Australian rule that design input must include Essential Principles when original product project was not thinking about Australian market. From what I heard you say, it seems that basic input is adherence to standards related to basic safety of device. Is this correct interpretation? Otherwise how does one remedy after the design phase when deciding to move into a new regulatory territory?
21. Could that be a quality plan to review all design docs and fill gap?
22. Do you grade and document a finding when there is already an open CAPA for it?

Who Will Benefit:

• CEO’s of companies, which sell to Australia, Brazil, Canada, Japan or US
• Regulatory Affairs Managers of Companies, which sell to Australia, Brazil, Canada, Japan or US
• Quality Managers of Companies, which sell to to Australia, Brazil, Canada, Japan or US
• Quality Representatives of Companies, which sell to Australia, Brazil, Canada, Japan or US
• Other managers, which need to deal with regulatory or quality guidelines
• Medical Device Manufacturers, who develop, manufacture and / or sell to US, CAN, BR, AUS, JP

Additional service: (Personalized session)

We also do various similar customized events for our clients and it is specially tailored as per the client's requirement. We arrange calls between clients and our course instructors to better understand the training requirement and accordingly a training program is designed. The course duration ranges between 90 Mins and 12 hours. Most 6 hours and 12 hours of classes are split into 2 to 3 days considering customer convenience.

We have 500+ consultants who are associated with us and each have their own specialization example GxP, GMP,GLP, 21 CFR, Computer system validation, FDA Audit & Inspection, Bioassays, Design Control, Data Integrity, FDA regulation, Clinical compliance, and almost everything that falls under Risk, Quality and Compliance arena in the Life Science industry.

If you think that your team needs some kind of boost, update or refresher in Risk management and Regulatory compliance then let me know and we can design a highly cost efficient program for you.