Dear All,
 
I would like to get consensus on how regulated industry (pharma and
non-pharma) handle archival submissions. That is, is there a system in
place to handle these? Are paper and/ or e-forms used? Is there a need
felt to maintain information on who and when something was submitted for
archiving, or just note that something has been received? What
regulations and/or standards are used?
 
Also, if bulk submissions are received, are there expectations that
inventories will accompany them, or is it just the responsibility of the
archivist? If so, is (and/ or how) is this enforced?
 
Many Thanks!

Judith T. Johnston 
Solvay Pharmaceuticals, Inc. 
*770-578-5840 
FAX: 770-578-5864 
http://www.solvaypharmaceuticals-us.com
<http://www.solvaypharmaceuticals-us.com/>  

 


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