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Reliable Guidance |
The Experts in Clinical Trial Materials Management™ |
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Document Control Systems
Approval Process of New and/or Existing Records
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Assignment of controlled document numbers
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Document process flow:
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Review
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Approval
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Distribution
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Retention
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Records Review Schedule
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Control of Official Copies, (i.e.: binder, working, reference & revision), including obsolete copies
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Documentation Control Roles and Responsibilities
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Please contact us regarding any of your Pharmaceutical, Biopharmaceutical, or Nutraceutical needs at:
6 Jacobs Lane, Scotch Plains, New Jersey 07076
Phone: (908) 233-4508 - Fax: (908) 654-4829
Email Us
© 2001-2007 Jeiven Pharmaceutical Consulting, Inc.
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