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Whether planning an impending IND submission, seeking expert safety oversight, or requesting comprehensive clinical trial proposals, our team responds promptly within 24 hours.

STUDY INQUIRY & RFP

Request a Clinical Trial Proposal

Please submit your study outline. All discussions and protocol synopses are protected by strict corporate confidentiality.

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General Inquiries

Our business development and medical directorates are available worldwide.

Hours: Mon–Fri, 8:30 AM – 6:00 PM EST
24/7 Safety & ICSR Reporting Hotline

For ongoing trial investigators reporting SUSARs, SAEs, or unexpected adverse drug events:

Hotline: +1 (800) 577-7233 | safety@astraclinical.com

Corporate Regional Contacts

North America (Montreal & Boston):
+1 (514) 934-0805 • na-trials@astraclinical.com
India & APAC (Mumbai & Faridabad):
+91 7738804988 • apac-trials@astraclinical.com
Europe & UK (London & Warsaw):
+44 20 7946 0912 • eu-trials@astraclinical.com
Latin America (Bogotá):
+57 1 744 3820 • latam-trials@astraclinical.com
Clinical Investigation Protocol Review
Study Proposal Received

Our Medical Review Team will contact you under NDA within 24 hours.