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Answer for What's the logic for document revision naming?​

The logic of revision naming is based on the following sequence of events
 

Routing Status
Revision
Change Log
Description

Draft
A
1
First draft of a document

Draft
A
2
Additional document revision was added without starting a routing process

In Work
A
2
Document Routing Process Started

Approved
A
2
Document is being Approved

Draft
B
1
A new document was added after document as being approved

Draft
B
2

Additional document revision was added without starting a routing process

Draft
B
3
Additional document revision was added without starting a routing process

In Work
B
3
Document Routing Process Started

Approved
B
3
Document is being Approved

 
NOTE: Document A.2 will turn to be Obsolete after B.3 will be approved

Author: Rami.Azulay

Expert in deployment of lifecycle management system into Medical Device vendors who seeking warranting successful Medical Device Auditing and Regulatory Compliance through Process Automation Tools It is no secret that Medical Device companies incur much costs and organizational stress relating to creating and maintaining their Technical File, DHF or ISO documentation, especially before first time submission or external auditing by notified bodies. https://il.linkedin.com/in/ramiazulay

Answer for What's the logic for document revision naming?​

The logic of revision naming is based on the following sequence of events
 

Routing Status
Revision
Change Log
Description

Draft
A
1
First draft of a document

Draft
A
2
Additional document revision was added without starting a routing process

In Work
A
2
Document Routing Process Started

Approved
A
2
Document is being Approved

Draft
B
1
A new document was added after document as being approved

Draft
B
2

Additional document revision was added without starting a routing process

Draft
B
3
Additional document revision was added without starting a routing process

In Work
B
3
Document Routing Process Started

Approved
B
3
Document is being Approved

 
NOTE: Document A.2 will turn to be Obsolete after B.3 will be approved

Author: Rami.Azulay

Expert in deployment of lifecycle management system into Medical Device vendors who seeking warranting successful Medical Device Auditing and Regulatory Compliance through Process Automation Tools It is no secret that Medical Device companies incur much costs and organizational stress relating to creating and maintaining their Technical File, DHF or ISO documentation, especially before first time submission or external auditing by notified bodies. https://il.linkedin.com/in/ramiazulay