• Toxicology Studies


  • Proactive planning ensures efficient risk management before, during and after the study
  • Each study is run by a dedicated Study Director and conducted by toxicologists with the right qualification, training, and experience
  • Independent quality assurance systems and checks guarantee consistent compliance with regulatory guidelines
  • An audit trail ensures complete access to raw a data generated during the study
  • Efficient cold chain maintained with data logger if organs or tissues are called for after the study
  • Allied services like test item stability, impurity analysis, and formulation development also available


Step 1

Document generation and control.

Step 2

Selection and training of Study Director and team.

Step 3

Test item import and determination of best dosage form.

Step 4

Dose finalization after balancing ethical norms and study objectives.

Step 5

Animal selection, randomization, and grouping.

Step 6

Facility inspection and qualification.

Step 7

Documentation audit and corrections.

Step 8

Master calibration of all instruments.

Step 9

Submitting reports at scheduled intervals.

Step 10

Double data entry.

Step 11

Analysis of biochemistry, histopathology, clinical chemistry using sensitive high-end instrumentation.

Step 12

Independent, comprehensive QA review of compliance.

Step 13

Publication for GRAS affirmation, NDI notification.

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