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Nonclinical Safety Testing Guide for a Successful Regulatory Submission

Unlock the Keys to Successful Preclinical Development

Ensuring the safety, stability, and compliance of your test article is critical for regulatory success. From dose formulation analysis to genetic toxicology testing, every step of preclinical development must be precise and validated. Access our free guide, where we dive into key considerations for your preclinical program:

• Test Article Formulation – Vehicle solubility, consistency, and stability verification
• Bioanalysis – FDA-compliant analytical validation for preclinical and clinical studies
• Toxicology & Safety Pharmacology – Required studies to support IND submissions
• SEND Compliance – Meeting regulatory data submission standards
• Choosing the Right CRO – GLP compliance, expertise, and regulatory history

Streamline your preclinical workflows and accelerate time to submission. 📥Download the full guide to learn more.

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