Veeva Quality Basics: QualityDocs on Veeva Basics Help

Mark Document as Final

Tue, 12 May 2026 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Control User

Document Control users can bypass the Quality Check of an Initial to Final document by marking it as Final.

To mark a document as Final:

Navigate to Document Workspace > Working Library and open the document you want to mark as Final.
Select Mark as Final from the Workflow Actions menu.
Click Yes to confirm.

Upload a New Version of a Document

Mon, 27 Apr 2026 00:00:00 +0000

Note Only Document Control, the document owner, and the QA approver of the document can create a draft from a steady state document.

Uploading a new version of a document often occurs when a steady state document reaches its periodic review on a document and the result is Needs Revision, or if a document needs to be reclassified but is already in the steady state.

Apply Overlay to a Protected PDF

Tue, 14 Apr 2026 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Vault Admin

Veeva recommends using the built-in system workflows to sign documents. However, you may bring protected documents into your Quality Vault that were signed outside of Vault.

In order to preserve the integrity of those protected documents, by default Vault will not apply overlays to protected documents. Vault Admins can choose to apply an overlay when generating the viewable rendition of a protected PDF.

Document External Approval

Tue, 14 Apr 2026 00:00:00 +0000

You can send documents following the Draft to Approved lifecycle for external approval.

This is helpful when you need a supplier to approve documents in your Vault.

Vault and Quality Admins can manage external approvers as contacts for an external organization.

If a contact is assigned as an external approver on a document:

When a document is sent for approval, if an external approver is specified as an approver, Vault will automatically create an account for them in the Active state.

How to Send a Document for External Approval

Tue, 14 Apr 2026 00:00:00 +0000

Time to complete: 3 minutes

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Delete a Document

Fri, 07 Nov 2025 00:00:00 +0000

Warning Attention Vault Admins: If one of the document’s versions is in a steady state, carefully follow all instructions so that you don’t accidentally delete all versions of the document, along with its history. Vault Admins have the ability to delete Approved documents for migration purposes.

Who can complete this task? Veeva Quality Basics: Vault Admin, Quality Admin, Document Control, Document Owner

Before deleting a document in Veeva Quality Basics, carefully read the instructions provided and make sure you are following the right instructions for your scenario.

Mark a Document as Ready for Approval

Mon, 27 Oct 2025 00:00:00 +0000

To mark a document as Ready for Approval:

From the Document Workspace > Working Library tab, open the document you want to mark as ready for approval.
From the Workflow Actions menu, select Mark as Ready for Approval.
Click Yes to confirm. Vault changes the document status to Ready for Approval.

Draft to Approved Documents

Sat, 25 Oct 2025 00:00:00 +0000

The Draft to Approved lifecycle is for document types that require the formal Approval process, but NOT the level of control facilitated by the Document Change Control process.

The following Documents Types follow this lifecycle:

Form > Electronic Executed Form
Operations > Agreement
Operations > Assessment
Operations > Certificate
Operations > Logbook
Operations > Memo
Operations > Method
Operations > Plan
Operations > Protocol
Operations > Report
Operations > Requirement
Operations > Safety Data Sheet

Task Sequence

Best Practice Complete tasks in the following order for Draft to Approved documents.

	Task	Who Does This Task
1	Create Draft	Full User	*If applicable
3	Send Document for Authoring/Review	Full User	*If applicable
4	Author/Review Document	Author(s)/Reviewer(s)	*If applicable
5	Send Document for Approval	Full User
6	Approve Document	Approver(s)
7	QA Approve Document	QA Approver(s)

Draft to Effective Documents

Sat, 25 Oct 2025 00:00:00 +0000

The Draft to Effective lifecycle is for the most controlled document types that are governed under the Document Change Control Process, which allows you to package several document changes into one approval process. This includes documents that will have an Issued period for training or require Periodic Reviews.

The following Documents Types follow this lifecycle:

All Governance and Procedure documents
Operations > Master Batch Record
Operations > Specification
Operations > Training Material
Form > Master Form Template

Task Sequence

Best Practice Complete tasks in the following order for Draft to Effective documents.

	Task	Who Does This Task
1	Create DCC	Full User
2	Create Draft(s)	Full User
3	Add Doc(s) to DCC	Full User
4	Send Doc(s) for Authoring/Review	Full User	*If applicable
5	Author/Review Doc(s)	Author(s)/Reviewer(s)	*If applicable
6	Mark Doc(s) Ready for Approval	Full User
7	Send DCC for Approval	Full User
8	Approve DCC	Approver(s)
9	QA Approve DCC	QA Approver(s)

How to Process a Draft to Approved Document

Sat, 25 Oct 2025 00:00:00 +0000

Time to complete: 2 minutes

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How to Process a Draft to Effective Document

Sat, 25 Oct 2025 00:00:00 +0000

Time to complete: 5 minutes

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How to Process an Initial to Final Document

Sat, 25 Oct 2025 00:00:00 +0000

Time to complete: 2 minutes

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Initial to Final Documents

Sat, 25 Oct 2025 00:00:00 +0000

The Initial to Final lifecycle is for documents that have been approved externally and are already in their Final version. This lifecycle allows documents to reach their steady state without going through an approval workflow.

The following Documents Types follow this lifecycle:

Executed Records
Form > Paper Executed Form
External Documents
All QMS Documents

Task Sequence

Best Practice Complete tasks in the following order for Initial to Final documents.

	Task	Who Does This Task
1	Create Draft	Full User
2	Send Document for QC	Full User
3	QC Review Document	QC Reviewer

Note Document Control Users can bypass the Quality Check for Initial to Final documents by marking the document as Final.

Perform a Periodic Review

Mon, 04 Aug 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Owner

When a document reaches its Periodic Review Date, a task is sent to the Document Owner for review.

Click the Document Periodic Review task.
Review the contents of the document to determine if it should remain effective, if changes are needed, or if it should be made obsolete. Click Complete to complete the task.

Preview eLearning Content

Mon, 04 Aug 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

To preview eLearning content:

Navigate to Document Workspace > Working Library and open an eLearning document.
Select Preview E-Learning Content from the Actions menu.
The eLearning opens in a new window. You can play through the course and view course information in the right pane.

Document Change Control Process

Wed, 09 Jul 2025 00:00:00 +0000

The Document Change Control Process allows you to package several document changes into one approval process. This includes, approval for the following:

New documents
Existing documents that require up-versioning
Existing documents that will become obsolete

Document Lifecycles

Wed, 09 Jul 2025 00:00:00 +0000

Once a document has been added to the Working Library, it can be processed through an appropriate lifecycle. The amount of control needed to move a document through an approval process determines which lifecycle it follows.

The following lifecycles are available and are dependent on the Document Type:

Initial to Final: This lifecycle provides limited document control.
Draft to Approved: This lifecycle provides document control through approvals.
Draft to Effective: This lifecycle provides the highest level of control and requires Document Change Control.

Reviewing and Approving Documents

Documents are sent through their respective lifeycle via the desired approval workflow:

Draft to Approved Lifecycle

Wed, 09 Jul 2025 00:00:00 +0000

The Draft to Approved lifecycle is for document types that require the formal Approval process, but NOT the level of control facilitated by the Document Change Control process.

The following Documents Types follow this lifecycle:

Form > Electronic Executed Form
Operations > Agreement
Operations > Assessment
Operations > Certificate
Operations > Logbook
Operations > Memo
Operations > Method
Operations > Plan
Operations > Protocol
Operations > Report
Operations > Requirement
Operations > Safety Data Sheet

Draft to Effective Lifecycle

Wed, 09 Jul 2025 00:00:00 +0000

The following Documents Types follow this lifecycle:

All Governance and Procedure documents
Operations > Master Batch Record
Operations > Specification
Operations > Training Material
Form > Master Form Template

Forms

Wed, 09 Jul 2025 00:00:00 +0000

Form refers to a document with fillable fields. In Veeva Quality Basics, you can create forms from a Master Form Template with the intention that they be completed electronically (Electronic Executed Forms) or on paper (Paper Executed Forms).

Master Form Templates

Intended to be an empty form containing the fields that you would like users to fill out
When created, Template Document Type can be set to either Electronic Executed Form or Paper Executed Form subtypes. You can also select Form, if the intention is to make it available for both subtypes.
Follow Draft to Effective lifecycle
Users can download the source file when the master form template is in Effective state

Template Document Types

When you create a Master Form Template, you can select from the following Template Document Types. Template Document Type identifies the type of document the master template should be available as a template once it reaches the Effective state.

Initial to Final Lifecycle

Wed, 09 Jul 2025 00:00:00 +0000

The following Documents Types follow this lifecycle:

Executed Records
Form > Paper Executed Form
External Documents
All QMS Documents

Non-GxP Documents

Wed, 09 Jul 2025 00:00:00 +0000

Veeva Quality Basics can be used to train users on non-GxP documents, such as corporate training materials.

There are two security profiles for users who should not access GxP content:

Non-GxP User - Allows users to create and participate with non-GxP documents only. Users with this security profile cannot access GxP content.
Non-GxP Read-Only User - Allows users to complete training on non-GxP documents only. Users with this security profile cannot access GxP content.

The Training Admin will manage the training matrix for both GxP and non-GxP documents.

Quality Basics: QualityDocs

Wed, 09 Jul 2025 00:00:00 +0000

Veeva Basics: QualityDocs is an application to manage documentation associated with a quality system, providing seamless collaboration, reducing compliance risk, and improving quality processes. It accelerates review and approval workflows, and facilitates sharing of GxP documents among employees.

Quality Relationships

Wed, 09 Jul 2025 00:00:00 +0000

You can open the Quality Relationships panel from the Document Info panel for a document.

The Quality Relationships panel has two sections: Training Requirements and Document Relationships.

Training Requirements

The Training Requirements section shows any training requirements that the document is a training material for.

Note This is version-specific. For example, if v1.0 of this document is a training material for a Training Requirement, it will show in this section. If you create a new draft, the Training Requirement section will be blank for v1.1. You do not need to create another Training Requirement for the draft version.

Associate a Supporting Document to a Document

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

Document relationships create a connection between two documents. In Veeva Quality Basics you can associate one or more supporting documents to a document. This type of relationship points to the latest version of a document.

Best Practice You should always add supporting documents to the Source document.

Example

This example shows an SOP. The References section has one document listed as a reference. To make the association between the SOP and the referenced document, you should:

Change a Document Owner

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Control Users and the current Document Owner

There may be times when you need to change the owner of a document, for example, if a user other than the current owner needs to update the document.

Note All documents need owners. If a document owner leaves your organization, make sure to assign a new document owner. Run the Documents with Inactive Owners report to find documents with an inactive owner.

To change the document owner of a document, refer to Update Sharing Settings.

Complete a Quality Check Task for a Document

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: QA User

Complete the following steps to complete a Quality Check task:

From the Document Workspace > Home tab, select the All Tasks view to view your assigned tasks.
Click Show more on the Quality Check task to view additional task information.
Click the document name or click Continue on the Quality Check task you need to complete. Vault opens the document and displays a task banner with the task due date and instructions.
Determine whether the document passes or fails the QC review and click Complete.
- If the document fails the QC, select Failed QC, enter a Reason for Failure, and click Complete. Vault marks the QC Review task complete and changes the document status back to Initial.
- If the document passes the QC, select Passed QC and click Complete. Vault marks the Quality Check task complete, changes the document status to Final, and displays the document in the Quality Consumer > Library tab.

Complete an Approval Task for a Document

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User, Non-GxP Document User, QA User

For documents in the Draft to Approved lifecycle, an Approval and QA Approval are both required before the document status is changed to Approved. The Approver must approve the document before the QA Document Approval task is assigned to the QA Approver.

Create a Binder

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Vault Admins and Quality Admins

Veeva Quality Basics will never require you to create binders for your documents. We provide powerful metadata and filters that enable you to find the documents you’re looking for, and keep those documents at your fingertips using views.

However, there may be some select scenarios where layered organization is needed and you want to use binders. In these scenarios, Admins can create a binder.

Create a Document

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

You can create new documents in Veeva Quality Basics using the following methods:

Upload a document from a drive
Create a placeholder document
Create a document from a template
Create a new draft of an approved document
Import a document that has been approved externally
See Supported File Formats to ensure that you’re using files of supported formats

Documents are numbered using VV-QUAL-XXXXX format and increment by 1.

Create a Document Change Control

Sun, 29 Jun 2025 00:00:00 +0000

You can use the Document Change Control feature to regulate the processes of creating a new draft, moving a draft into its steady state (releasing it for use), or withdrawing an existing, approved document.

To create a document change control:

Navigate to Document Workspace > Document Change Controls and click Create.
Fill out the required information.

Note Implementation Period (Days) indicates the number of calendar days after approval that the documents in the DCC become Effective or Obsolete. Enter 0 if the change can be implemented immediately.
Click Save.

Create a Document Template

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

Document templates allow you to quickly create new documents from a configured template. When you create a new document from a template, Vault copies the template file and uses that copy as the source file for the new document. This process bypasses the content upload process and allows for more consistent document creation.

Create a Non-GxP Document

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

Veeva Quality Basics can be used to train users on non-GxP documents, such as corporate training materials. Non-GxP documents must have a document type of Operations Training Material.

To create a non-GxP document:

Navigate Document Workspace > Working Library and click Create.

Import Preapproved Legacy Content

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Vault Admins and Quality Admins

Import Internal Documents

Follow these steps to import internal documents, i.e., those you will manage and upversion in Vault, like SOPs.

To import preapproved internal documents:

Navigate to Document Workspace > Working Library and click Create.
Select Upload and click Continue.

Mark a Document Confidential

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

The Confidential? field controls visibility of documents.

If Confidential? is answered Yes, Vault Admins, Quality Admins, and Document Control Users can see the document. Other users can see confidential documents only when assigned a task or manually added as a Viewer.

If Confidential? is answered No, users will be able to see the document in its steady state.

Reclassify a Document

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? You can only reclassify a document when it is in Draft state. If the document you need to reclassify is in a steady state, create a new draft.

To reclassify a Document:

Navigate to Document Workspace > Working Library, and open the document you want to edit.
Click Reclassify in the Information panel, select a new Type, Subtype, and Classification, and click OK.

Review a Document Change Control

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics users identified as an Approver or QA Approver of a Document Change Control (DCC)

Document Change Controls can contain items to be made Effective as well as Obsolete. To complete the DCC process, reviewers must assess and confirm both.

Note The approval due date is specified when the DCC is created. To make sure that QA has enough time to complete their task before the due date, the first level approval due date is calculated to be the Approval Due Date minus 3 days.

To review a document change control:

Send a Document for Approval

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User, Non-GxP Document User

Send a Document for Approval

To send a Draft or Ready for Approval document for approval:

Navigate to Document Workspace > Working Library and open the document you want to send for approval.
Select Send for Approval from the Workflow menu.

Send a Document for Obsolescence Approval

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User, Non-GxP Document User

Send a Document for Obsolescence Approval

To send a Ready for Approval document for obsolescence approval:

Navigate to Document Workspace > Working Library and open the document you want to send for obsolescence approval.
Select Send for Obsolescence Approval from the Workflow menu.

Send a Document for QC Review

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User, Non-GxP Document User

Complete the following steps to send an Initial document for QC review:

From the Document Workspace > Working Library tab, open the document you want to send for review.
Select Send for QC from the Workflow Actions menu.
In the Start Workflow dialog, select the QC Reviewers. All Reviewers must complete their QC before the document can be moved to Final.
Enter a Due Date for completion of the QC review and click Start. Vault changes the document status to In QC and assigns a Quality Check task to the selected reviewers.

Send a Non-GxP Document for Approval

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

Non-GxP documents follow a modified Draft to Effective Lifecycle. Unlike GxP training materials, they do not go through document change control. When it’s ready to be approved, you can send it for non-GxP approval.

Non-GxP Document Approval

To send a non-GxP document for approval:

Use Merge Fields for Microsoft Word & Excel

Sun, 29 Jun 2025 00:00:00 +0000

Who can complete this task? Veeva Quality Basics: Document Workspace User

Using the Merge Fields, you can trigger Vault to search within a Microsoft Word (DOCX only) or Microsoft Excel (XLSX) source file and replace certain tokens with field values from the Vault document. Merging fields can make it easy to create templates that auto-populate with details like product name, document status, and version date. You can also use this to add a title page to a document that shows the document name or document number from the Vault.

Veeva Quality Basics Document Categories

Sun, 29 Jun 2025 00:00:00 +0000

Name	Category	Sub-Category
Agreement-Quality	Agreement	Quality
Agreement-Service	Agreement	Service
Agreement-Technical	Agreement	Technical
Assessment-Compliance	Assessment	Compliance
Assessment-Gap	Assessment	Gap
Assessment-Impact	Assessment	Impact
Assessment-Risk	Assessment	Risk
Certificate-Analysis	Certificate	Analysis
Certificate-Cleaning	Certificate	Cleaning
Certificate-Compliance	Certificate	Compliance
Certificate-Conformance	Certificate	Conformance
Certificate-Destruction	Certificate	Destruction
Certificate-Disposition	Certificate	Disposition
Certificate-Labeling	Certificate	Labeling
Certificate-Packaging	Certificate	Packaging
Certificate-Qualification	Certificate	Qualification
Certificate-Review	Certificate	Review
Certificate-Supplier	Certificate	Supplier
Certificate-Test	Certificate	Test
Executed Record-Clinical	Executed Record	Clinical
Executed Record-Disposition	Executed Record	Disposition
Executed Record-Executed Batch Record	Executed Record	Executed Batch Record
Executed Record-Labeling	Executed Record	Labeling
Executed Record-Non-Clinical	Executed Record	Non-Clinical
Executed Record-Packaging	Executed Record	Packaging
Executed Record-Quality	Executed Record	Quality
Executed Record-Test	Executed Record	Test
Executed Record-Training	Executed Record	Training
Executed Record-Transportation	Executed Record	Transportation
Memo-Appointment	Memo	Appointment
Memo-Approval	Memo	Approval
Memo-Clarification	Memo	Clarification
Memo-Clinical	Memo	Clinical
Memo-Computerized Systems	Memo	Computerized Systems
Memo-Justification	Memo	Justification
Memo-Note to File	Memo	Note to File
Memo-Quality	Memo	Quality
Memo-Regulatory	Memo	Regulatory
Memo-Validation	Memo	Validation
Method-Cleaning	Method	Cleaning
Method-Equipment	Method	Equipment
Method-Process	Method	Process
Method-Raw Material	Method	Raw Material
Method-Test	Method	Test
Plan-Clinical	Plan	Clinical
Plan-Quality	Plan	Quality
Plan-Test	Plan	Test
Plan-Validation	Plan	Validation
Protocol-Analytical	Protocol	Analytical
Protocol-Clinical	Protocol	Clinical
Protocol-Development	Protocol	Development
Protocol-Equipment	Protocol	Equipment
Protocol-Non-Clinical	Protocol	Non-Clinical
Protocol-Process	Protocol	Process
Protocol-Quality	Protocol	Quality
Protocol-Stability	Protocol	Stability
Protocol-Test	Protocol	Test
Protocol-Validation	Protocol	Validation
Report-Analytical	Report	Analytical
Report-Clinical	Report	Clinical
Report-Computerized Systems	Report	Computerized Systems
Report-Development	Report	Development
Report-Disposition	Report	Disposition
Report-Equipment	Report	Equipment
Report-Non-Clinical	Report	Non-Clinical
Report-Qualification	Report	Qualification
Report-Quality	Report	Quality
Report-Stability	Report	Stability
Report-Transportation	Report	Transportation
Report-Validation	Report	Validation
Requirement-Functional	Requirement	Functional
Requirement-User	Requirement	User
Specification-API (DS)	Specification	API (DS)
Specification-Design	Specification	Design
Specification-Environment	Specification	Environment
Specification-Equipment	Specification	Equipment
Specification-Excipient	Specification	Excipient
Specification-Labeling	Specification	Labeling
Specification-Packaging	Specification	Packaging
Specification-Process	Specification	Process
Specification-Processing Aid	Specification	Processing Aid
Specification-Product	Specification	Product
Specification-Raw Material	Specification	Raw Material
Specification-Reference Standard	Specification	Reference Standard
Specification-Substance	Specification	Substance
Standard Operating Procedure (SOP)-Analytical	Standard Operating Procedure (SOP)	Analytical
Standard Operating Procedure (SOP)-Clinical	Standard Operating Procedure (SOP)	Clinical
Standard Operating Procedure (SOP)-Computerized Systems	Standard Operating Procedure (SOP)	Computerized Systems
Standard Operating Procedure (SOP)-Data Management	Standard Operating Procedure (SOP)	Data Management
Standard Operating Procedure (SOP)-Development	Standard Operating Procedure (SOP)	Development
Standard Operating Procedure (SOP)-Equipment	Standard Operating Procedure (SOP)	Equipment
Standard Operating Procedure (SOP)-Facility	Standard Operating Procedure (SOP)	Facility
Standard Operating Procedure (SOP)-Manufacturing	Standard Operating Procedure (SOP)	Manufacturing
Standard Operating Procedure (SOP)-Non-Clinical	Standard Operating Procedure (SOP)	Non-Clinical
Standard Operating Procedure (SOP)-Process	Standard Operating Procedure (SOP)	Process
Standard Operating Procedure (SOP)-Quality	Standard Operating Procedure (SOP)	Quality
Standard Operating Procedure (SOP)-Regulatory	Standard Operating Procedure (SOP)	Regulatory
Standard Operating Procedure (SOP)-Safety	Standard Operating Procedure (SOP)	Safety
Standard Operating Procedure (SOP)-Stability	Standard Operating Procedure (SOP)	Stability
Standard Operating Procedure (SOP)-Supply Chain Management	Standard Operating Procedure (SOP)	Supply Chain Management
Standard Operating Procedure (SOP)-Validation	Standard Operating Procedure (SOP)	Validation
Training Material-Clinical	Training Material	Clinical
Training Material-Corporate	Training Material	Corporate
Training Material-Course	Training Material	Course
Training Material-User	Training Material	User

Veeva Quality Basics Document Types

Sun, 29 Jun 2025 00:00:00 +0000

Document Type	Subtype	Available Lifecycle
Executed Record		Initial to Final
External Document		Initial to Final
Form	Paper Executed Form	Initial to Final
Form	Electronic Executed Form	Draft to Approved
Form	Master Form Template	Draft to Effective
Governance and Procedure	Guidance	Draft to Effective
Governance and Procedure	Job Aid	Draft to Effective
Governance and Procedure	Master Template	Draft to Effective
Governance and Procedure	Policy	Draft to Effective
Governance and Procedure	Quality Manual	Draft to Effective
Governance and Procedure	Standard	Draft to Effective
Governance and Procedure	Standard Operating Procedure (SOP)	Draft to Effective
Governance and Procedure	Work Instruction	Draft to Effective
Operations	Agreement	Draft to Approved
Operations	Assessment	Draft to Approved
Operations	Certificate	Draft to Approved
Operations	Logbook	Draft to Approved
Operations	Master Batch Record	Draft to Effective
Operations	Memo	Draft to Approved
Operations	Method	Draft to Approved
Operations	Plan	Draft to Approved
Operations	Protocol	Draft to Approved
Operations	Report	Draft to Approved
Operations	Requirement	Draft to Approved
Operations	Safety Data Sheet	Draft to Approved
Operations	Specification	Draft to Effective
Operations	Training Material	Draft to Effective
QMS Document	Audit Agenda	QMS Initial to Final
QMS Document	Audit Certificate	QMS Initial to Final
QMS Document	Audit Program	QMS Initial to Final
QMS Document	Audit Report	QMS Initial to Final
QMS Document	Audit Response	QMS Initial to Final
QMS Document	Change Control	QMS Initial to Final
QMS Document	Complaint	QMS Initial to Final
QMS Document	Deviation	QMS Initial to Final
QMS Document	Lab Investigation	QMS Initial to Final
QMS Document	Standalone CAPA	QMS Initial to Final
QMS Document	Supplier Qualification	QMS Initial to Final