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TEKLYNX CENTRAL CFR has been leveraged from a solid application platform and wrapped with functionality to provide seamless integration into the entire regulated enterprise. Pharmaceutical companies, high-volume laboratories and other organizations that require a robust Quality Management System will find that Validation of this new product in their end-user environment is extremely straight forward.
- Tony Raymond,Consultant/President of New Harbor SQA
Applications
- Medicine and drug labeling
- Drug component identification
- Food & Drug Administration (FDA) 21 CFR Part 11 compliance
- Lab sample tracking
- Medical device identification
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Valued Partners
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Microsoft Gold Certified Partner
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Oracle Gold Partner