THE VEDIC ADVANTAGE
- 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.
