For over 23 years, Hurley Consulting Associates, Ltd. has specialized in "Finding Solutions" for its clients' regulatory and overall drug development needs. Using our unique expertise, we integrate nonclinical, clinical, and CMC evaluations; perform data analyses; and develop and implement regulatory strategies to provide the highest quality documents and dossiers for global submissions. For further information on our services, please visit our website at www.hurleyconsulting.com.
Chemistry/Manufacturing/Controls Clinical Trial Monitoring Data Validation Drug Master File Dossiers Electronic Submissions Medical Writing Nonclinical Pharmacology Programming (Database/SAS/etc) Regulatory Affairs/Regulatory Strategy Statistical Services/Meta Analysis
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