June 22, 2007
Word for the Wise
"It takes 20 years of hard work to become an overnight success."
--Diana Rankin,
writer and public speaker
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Welcome To Z-Teck Consulting!
Z-TECK provides comprehensive regulatory and quality system assistance to help firms meet domestic and international product requirements. Z-TECK assures high quality, reliability, and integrity in the performance of its services.
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Quality Audits ...
A third-party independent audit can add credibility to your credentials and improve your quality system by taking appropriate corrective actions to observations. Audits to U.S. drug cGMP and the medical device Quality System Regulation, and to the European ISO/EN 13485 medical device standard can be scheduled at your convenience. Read More. . . -login- |
Clinical study FDA and societal pressures demand robust clinical trials . Z-Teck coordinates and oversees clinical investigations from concept to publication. Contact Z-Teck for assistance with protocol development, IRB documentation and approvals, clinical investigator contracts, investigator brochures, and IND and IDE submissions.
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