Seerpharma.com.au :: Pharmaceutical Consulting & Training :: Validation, GMP & Compliance UK | Singapore

   

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Document management for R&D

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Product description

Seerpharma has developed a document management solution specifically for R&D organizations to secure and manage your high value development documentation using EtQ Reliance™ web based software.

Product features

  • manage electronic and hard copy documents from all sources
  • full audit trail and ability to QC documents entered in to the system
  • capability to manage controlled documents and records (with archive function)
  • record document locations and distribution
  • categorize and search for documentation
  • store information relating to contractors
  • ability to restrict access to documents
  • ability to create unique document numbers in any format
  • automatically package documents for electronic distribution
  • version control capability including change process for controlled documents
  • ability to access the system from anywhere in the world (assumes appropriate security access)
  • ability to electronically review and approve documents (21 CFR 11 compliant)

Product benefits

  • secure and manage documentation to facilitate;
    • ongoing product development
    • preparation of regulatory dossiers (e.g. IMPD, IND, NDA)
    • in/out licensing, partnering and associated due diligence
    • technical transfer, process optimization and scale up
  • never lose a document …no time wasted searching for documents
  • know what documents have been received and distributed
   

For more information

Australia:

iqa@seerpharma.com.au
+61 418 849 791

Singapore: David Grennan
+65 6774 5800

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