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  FORMULATION DEVELOPMENT :: QA & Documentation
Fusion Scientific Laboratories QA team is competent to handle all documentation on
  1. SOP Preparation & Periodical review of SOP’s
  2. System Implementation
  3. Independently monitors all the activities to ensure compliance to protocol, SOP’s, GLP and other regulations
  4. All Regulatory submissions
  5. Out of specification results and atypical results
  6. Change controls
  7. Internal Audits
  8. Training
  9. Cleaning verification
  10. Quality Manual
  11. Destruction of material
  12. Licenses and
  13. Handling of Deviations
Documentation
All documents sent to clients are checked and approved by Quality Assurance and records (hard copies & soft copies) of all the documents are archived.
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