Medtech Insight is part of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction
UsernamePublicRestriction

Compliance Corner: Leverage MDSAP Companion Doc To Master Your Next Audit, Train Staff, Expert Advises

Executive Summary

Longtime industry expert Connie Hoy says medtech companies that sign up for an audit through the Medical Device Single Audit Program will have a leg-up if they prepare beforehand by reading the MDSAP Companion Document. The doc can also be used to train workers on what an MDSAP auditor will be looking at and asking for.

Medtech companies that sign up for an audit through the Medical Device Single Audit Program will have a leg-up if they prepare beforehand by reading the MDSAP Companion Document and training staff on its relevant parts, an industry expert advises.

MDSAP, created by the International Medical Device Regulators Forum (IMDRF), allows firms to undergo one audit by an accredited third party to satisfy quality regulations for the US, Canada, Brazil, Japan and Australia. The auditing approach maps to international quality systems standard ISO 13485.

Similar in spirit to the US Food and Drug Administration’s Quality System Inspection Technique (QSIT) for agency investigators, the 123-page companion doc details how an MDSAP audit unfolds. It outlines the processes that auditors will focus on during an audit and the tasks – or steps – they must accomplish when reviewing a particular area.

“The companion document lays out, word-for-word, what questions you’re going to be asked by the auditor, in what order they’re going to be asked, and what objective evidence they’re going to want to look at,” said Connie Hoy of Hoy & Associates Regulatory Consulting.

“What more could you possibly want to be prepared?” – Connie Hoy

Hoy, who previously was executive VP of clinical development and regulatory affairs for device maker Cynosure, said manufacturers that read and digest the document will have an advantage by understanding in advance the general direction of the audit, as well as where any gaps might lie in their quality system.

“When I [worked at Cynosure and] got my hands on the companion document, I was really happy. It looked very familiar because it follows ISO 13485,” Hoy said.

“But I was very, very happy that the document lays out, ‘First they’re going to ask you this, and then they’re going to want to look at this piece of objective evidence, and then they’re going to move on and link it to another process, and ask you this, and look at this objective evidence,’” she said. “What more could you possibly want to be prepared?”

Hoy also urges device makers to use the companion doc as an MDSAP training tool.

“So, make sure you read this document,” she said. “You want to read it, and read it, and read it. You want to highlight sections. Highlight the things you think you’re missing. And use it as a training tool – but don’t give it to everybody in your company.”

That’s because handing out such a large document could prove intimidating for workers.

The companion doc “is more than a hundred pages of ‘Oh my gosh’ – and if you’re an engineer and you’re not used to reading that type of document, it can be daunting. So you don’t want to just give them the entire thing.”

Instead, Hoy recommends that firms use software like Adobe to cut and paste relevant sections into a smaller, easier-to-digest document.

“By doing that, I created training tools right out of the companion document,” she said. “And so when I met with purchasing, for example, and said, ‘OK guys, this what the MDSAP auditor is going to be looking at,’ I didn’t give them a hundred pages – I gave them seven, and used it as my training tool to help train my organization.”

Hoy’s comments came during FDAnews’ 14th Annual FDA Inspections Summit.

 

Topics

Key Documents

UsernamePublicRestriction

Register

ID1122310

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel