ISO 13485:2016 Section | Document Section |
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4.2.4 | (All) |
4.2.5 | (All) |
This SOP describes how documents and records are handled. The goal is to understand how documents are typically structured and their current state as they move from draft to release. The most recent document must be available at a specified location while ensuring changes to documents are always traceable.
Process Owner | <enter role of process owner> |
Key Performance Indicators | <enter KPIs to be tracked for the Management Review> |
This whole template assumes that you’re using Google Drive and Google Docs for your QMS. If you’re using something else, then.. good luck. Just kidding. You need to customize it, of course. There’s specialized QMS software out there which makes some of these tasks easier and lots of other tasks harder :) Make sure to describe somewhere (ideally in this first paragraph), in which tool your QMS documents will be managed and stored.
Documents are expected to change over time, whereas records are created once and not altered significantly afterwards.
All documents are written in English.
Documents are named according to this schema:
ASSOCIATED PROCESS-TYPE-NAME
Where “associated process” can be abbreviated in capital letters and “type” refers to an abbreviation of the document type (see below). “Name” refers to the actual file name.
Example: SWD-SOP-Integrated Software Development
For released documents, we add a “-a” suffix (as in: approved) to the document name.
Example: SWD-SOP-Integrated Software Development-a
For archived documents, we add a “-archived_ARCHIVE DATE” suffix to the document name.
Example:
SWD-SOP-Integrated Software Development-archived_2021-03-01
Product records are labeled with a device number, device version and associated process.
Example: PR1-V1.2-SWD-SWDP-Software Development Plan
There probably will be more types in the future when I add more templates. For now, this covers all types of the templates on openregulatory.com.
Abbreviation | Description |
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AM | Attachment |
LIS | List |
SD | Supporting Documentation |
SOP | Standard Operating Procedure (Process Description) |
TPL | Template |
QMS documents and records shall be stored for at least 10 years after their archival date.
Technical Documentation shall be stored for at least 10 years after the lifecycle of the respective device has ended.
We check our QMS documents regularly following a risk-based approach in order to ensure they remain up to date:
We keep an overview list of all QMS documents, including document type, release date, next review date and respective process owners.
This assumes you have three folders in your GDrive: “drafts”, “under review” and “released”.
All documents are saved in the Quality Management System (QMS) which is a folder in Google Drive.
New documents can be created by anyone in the company in the “drafts” folder. Naming of documents follows the general considerations of this SOP (see above). Standard Operating Procedures (SOP) should specify a process owner responsible for typically updating, reviewing and releasing all associated documents.
Participants |
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Any employee |
Input | Output |
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Content | New Document (draft) |
Once a document is ready for review, its author moves it to the “under review” folder. Importantly, the author selects appropriate reviewers and approvers and notes them at the bottom of the document.
Participants |
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Any employee |
Input | Output |
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Document (draft) | Document (under review) |
The respective reviewer(s) and approver(s) review the document. If changes are required, they create comments in the Google Doc and/or suggest changes. If the review is successful, they sign their initials at the bottom of the document.
Participants |
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Process owner and/or designated reviewer(s) and approver(s) |
Input | Output |
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Document (under review) | Document (review successful) |
The Process Owner moves the document to the “released” folder and assigns “-a” to the document name as outlined by the general considerations for document naming.
Access to the “released” folder is restricted to prevent unauthorized changes to released documentation.
The QMO (and, if applicable, the process owner) decide if employee training is required. In general, training for minor changes/corrections is not necessary.
Participants |
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QMO, Process Owner |
Input | Output |
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Document (review successful) | Document (released) |
If changes need to be made to a document, any employee with knowledge about the document and those changes can perform them. For that, the currently-released document is copied to the “drafts” folder and edited by the employee. After finishing the edit, it moves to the Document Ready for Review stage (step 2), following the same steps as above.
Changes to documents should be reviewed and approved by the original author, process owner or by a designated role with sufficient background information to make a qualified decision.
A QMS document change can trigger a substantial change. Before release, it shall be checked whether it may impact the organization’s process landscape and hence, overall organizational conformity with regulatory requirements. The QMO is responsible to evaluate such potentially major changes as part of the Change Evaluation List (reference change management process).
Participants |
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QMO, any employee |
Input | Output |
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Document (released) | Document Copy (draft) |
Documents get archived if they become obsolete or a newer released version becomes available. For that, the Process Owner removes the “-a” suffix, moves the document to the “archive” folder and assigns a respective archiving date following the general considerations for document naming in this SOP. We observe retention periods as outlined in this SOP and delete documents as soon as the retention period expired.
Participants |
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Process Owner |
Input | Output |
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Document (released) | Document (archived) |
We create records as required by our processes. If available, we use templates and checklists for the creation of records. Naming conventions as outlined for documents do not apply. Records should include an author’s name and the date of creation.
Participants |
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Any employee |
Input | Output |
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Content, Template Document (if applicable) | New Record |
Unless specified differently in a template or SOP, records do not typically require a review and release process.
Participants |
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Designated reviewer(s) and approver(s) |
Input | Output |
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Record (under review) | Record (review successful) |
Records are not necessarily stored in our QMS folder. They also may reside in other applications as specified per respective processes. This is where records are typically stored:
Add all your tools which stores data which is mentioned in your QMS.
Records are not significantly altered after creation / release. Where significant changes are required, we rather create a new record and archive the old one. Non-substantial changes (e.g. spelling mistakes) are considered corrections only, assessed and added on a case-by-case basis.
Participants |
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Any employee |
Input | Output |
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Record (released) | Record (updated) |
Records are archived if they become obsolete or a new released version becomes available. For that, the process owner moves the records to a respective archiving location. If possible, we follow the general considerations for document names and add the archiving date to the record name. We observe retention periods as outlined in this SOP and delete records as soon as the retention period expired.
Participants |
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Process Owner |
Input | Output |
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Record (released) | Record (archived) |
Template Copyright openregulatory.com. See template license.
Please don’t remove this notice even if you’ve modified contents of this template.