FDA Clarifies The Types Of MDSAP Audits To Be Conducted In The Pandemic

by | Jan 27, 2021 | AI, Audits, Coronavirus, COVID-19, FDA, MDSAP, Quality, Regulatory

The FDA released an information transmittal to the MDSAP Auditing Organizations on December 31st, 2020 providing further guidance on the expansion of remote MDSAP audits during the period of the public health emergency.1

Under this transmittal order, FDA clarifies the difference between the following types of audits and defines when such an audit would be appropriate. Below are the types of audits defined in this order:1

  • Desktop Audit: An audit performed remotely by reviewing documentation.
  • Remote audit: An audit performed off-site using information and communication technology (ICT).
  • Hybrid audit: An audit partially performed off-site using ICT while at least one MDSAP qualified auditor is simultaneously on-site during a portion of the audit.
  • Surrogate Audit: An audit partially performed off-site using ICT while at least one non-MDSAP qualified auditor is simultaneously on-site during a portion of the audit.

 

As per this order, an audit conducted based on ICT will not be an option for a facility whose previous remote audit was deemed ineffective.1

The order further states that, the eligibility of a facility for alternative audit arrangements will be based on a risk assessment that takes the facility’s compliance history, the medical devices produced, and the production technologies employed at the facility into consideration.1

According to this risk-based system, a stage 1 remote audit can be conducted for all risk categories, however, a remote stage 2 audit can only be conducted for low or medium risk companies. Stage 2 audit for high-risk companies must at least be a hybrid audit if not on-site.1

In the case where a facility is ineligible for any of the audit arrangements defined above, and an on-site audit cannot be performed, auditing organizations have the right to consider suspension or withdrawal of their certificates.1

Furthermore, certifications renewed with a remote audit will have a validity period of not to exceed twelve (12) months and shall be subject to subsequent on-site verification as

soon as possible. Certificates that were renewed in 2020 through a remote audit may have their validity extended for a further 12 months if on-site verification is not possible, however, ongoing surveillance must be carried out using alternative methods.1

 

It is interesting to see how the pandemic has given rise to these new definitions in the auditing world. This is certainly going to change how audits will be conducted in the future. Has this new auditing practice impacted you? Call us at +1 248-987-4497 or email us at info@emmainternational.com to know more about the auditing services we have to offer for your organization.


1DA (Dec 2020) MDSAP Transmittal Number: AO 2020-10 retrieved on 1/24/2021 from https://www.fda.gov/media/144883/download

 

Nikita Angane

Nikita Angane

Solutions Delivery Specialist - Ms. Angane is a Bioengineering graduate with experience in medical device commercialization, product development, quality system compliance and regulatory affairs. Her portfolio includes working on medical devices, combination products, and pharmaceuticals. As a Solutions Delivery Specialist at EMMA International, she offers her expertise to help our clients achieve an effective and sustainable quality system, and develop regulatory strategies for market access and compliance of new products in the US and international markets. Ms. Angane earned a Bachelor of Engineering in Biomedical Engineering from the University of Mumbai, India and an M.S. in Bioengineering from University of Illinois at Chicago.

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