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Information Systems Division
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Regulatory

Quality Assurance & Scientific Support
Establish GLP Programs
Third-Party GCP Auditors
Supporting Existing QAU
Scientific Support & SOP Development
Training Programs
21 CFR Part 11
GLP Archiving
 
 
 
 
Regulatory

You face tremendous pressure - internal as well as external - in trying to rapidly bring products to market, decrease cycle time, ensure compliance, and increase productivity. We can help you dramatically improve your efforts as a result of the expertise we've gained working with most of the top "players" in the life sciences field as well as with all the regulatory agencies. Our solutions are used by FDA and EPA processing centers as well as the world's top pharmaceutical companies and many organizations in the biotechnology, agrochemical, and research and manufacturing fields.

Common Applications:
  • Electronic submissions
  • Compliance management (Sarbanes-Oxley and Check 21)
  • Research programs
  • Library/Archive management


 
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