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ISO 22716 Checklist

ISO 22716 2017 version Checklist

The ISO 22716 checklist is organized according to the chapters of the standard, to ensure a complete assessment of all requirements of the new standard.

22716:2017 Transition Checklist

If you are thinking of preparing an ISO 22716 2017 version for good manufacturing practices (GMP) for the cosmetics manufacturing industry then where do you start? 

We start with a Gap Analysis to determine the gap between your current Management System (GMP) and an ISO 22716 2017 for good manufacturing practices (GMP) for the cosmetics . A Gap Analysis is used to assess an organization’s scope, readiness, and resources for building the Cosmetics Management System. It also provides us with the data to develop a project plan for ISO 22716 GMP implementation.

This gap analysis checklist can be used in evaluating your Management System (MS) against the requirements of ISO 22716:2017.

 

ISO 22716 checklist is considered a very good tool for auditors to make an audit questionnaire to verify the effectiveness of the implemented Cosmetics Management System. A total of more than 100 internal ISO 22716 audit requirements are prepared based on ISO 22716:2017 standard.

 

This ISO 22716 checklist shall be filled in by the business that are applying for, or wish to renew its certification. If a certified business has made big changes in the management system’s structure, the ISO 22716 checklist also shall be filled in.

The paragraphs arranged in the ISO 22716 checklist are in the same order as given in the official standard. In some cases, they are also referred to as other required documents.

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Hence, we were able to finish all tasks within our expected timeframe. From developing a quality manual to updating control of documents, QSE Academy made sure their consultants were always assisting”

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Quality Manager​

“Our business wanted to create an ISO 22716 quality manual, but we were on a tight budget. Fortunately, QSE Academy offered half the amount other firms were expecting us to pay. Not only did we avoid hefty expenses, but we also saved time and effort in complying with the standard.”

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Quality Manager

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