Aclairo® Pharmaceutical Development Group, Inc. is committed to delivering independent and objective nonclinical and regulatory advice to the pharmaceutical industry. Every member of Aclairo’s staff strives to provide our clients with superior advice, analysis, work product and program assistance.

Aclairo’s unique experience and capabilities help our clients’ development programs succeed. Our senior consultants are experienced ex-FDA or industry specialists and can provide expert guidance in the areas of toxicology, regulatory, ADME and clinical pharmacology drug development. In addition, our scientific services group can provide full program management and study monitoring and are experienced in supporting the gamut of regulatory document preparations including: Final Study Reports; Regulatory Applications; Investigator Brochures; Expert Reports; and FDA Response Documents