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I am searching for some advice on document control. I have thumbed through the related threads, procedure attachments, etc...yet I think some advice on my specific situation would be more helpful.
So, here it is...we are a materials testing laboratory, as such we maintain a vast library of technical specifications ASTMs, Client Specs, Material specs, MIL stds, FED, etc...Suffice it to say we have thousands of technical specifications in hardcopies. The trick is keeping these updated to their most current revision levels. Some, we get notifications on, such as the ASTMs whenever a revision occurs, others (specifically client specs) we have to review the revision level to assure we have the correct level.
What's worse, is this is compounded, since each spec is digested for core requirements (particular to our testing) and is placed into a master lab test document, so additionally we have to ensure these master documents are also correct to the most current revision level.
This process, when you factor in how many specs were talking about, is prone to errors. Additionally, upkeep of the specifications is beyond cumbersome. I wonder if anyone has experience managing a document control system like this. I'm looking for any advice on how to simplify this process, minimize the likelyhood that any outdated specifications will be utilized.
Currently we somewhat rely on the customer to dictate what spec and revision level needs to be used, verifying that the master lab sheet is current, proceeding if it is, and updating the document/spec if it's not. However, the majority of clients do not list revision levels, or they list revision levels that are outdated without their knowledge. Relying on the customer for this is not an acceptable form of control.
Hoping to find a better way to proceed without throwing gobs of manpower at the documents control program...

So, here it is...we are a materials testing laboratory, as such we maintain a vast library of technical specifications ASTMs, Client Specs, Material specs, MIL stds, FED, etc...Suffice it to say we have thousands of technical specifications in hardcopies. The trick is keeping these updated to their most current revision levels. Some, we get notifications on, such as the ASTMs whenever a revision occurs, others (specifically client specs) we have to review the revision level to assure we have the correct level.
What's worse, is this is compounded, since each spec is digested for core requirements (particular to our testing) and is placed into a master lab test document, so additionally we have to ensure these master documents are also correct to the most current revision level.
This process, when you factor in how many specs were talking about, is prone to errors. Additionally, upkeep of the specifications is beyond cumbersome. I wonder if anyone has experience managing a document control system like this. I'm looking for any advice on how to simplify this process, minimize the likelyhood that any outdated specifications will be utilized.
Currently we somewhat rely on the customer to dictate what spec and revision level needs to be used, verifying that the master lab sheet is current, proceeding if it is, and updating the document/spec if it's not. However, the majority of clients do not list revision levels, or they list revision levels that are outdated without their knowledge. Relying on the customer for this is not an acceptable form of control.
Hoping to find a better way to proceed without throwing gobs of manpower at the documents control program...
