NETS - GLP Preclinical Studies
What are GLP preclinical studies and why are they important in drug development?
Unlike the early phases of nonclinical research, later pharmacology and toxicology studies should be completed using the recommended documentation procedures found in the GLP (Good Laboratory Practices) standards. GLP standards aim to produce records of experiments that are suitable for regulatory organizations, ensuring that the submitted data has been obtained using proper, thoroughly documented procedures.
Testimonials: How we did it
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