Quality Policy Inspections & Compliance Certificates EHS

Arch Pharmalabs Avon GMP manufacturing facility (Solapur, Maharashtra) successfully received a USFDA audit and is approved for supply of a bulk API. Our Vitalife GMP manufacturing unit expects a USFDA inspection in 2009 and has successfully received more than 7 full GMP / QA audits from global majors, including Top 10 companies. In addition, Arch Pharmalabs routinely receives GMP / GLP / EHS audits in preparation for site registration from current and prospective customers from across the world. All Arch Pharmalabs sites have ISO 9001:2000 or ISO 140001 certifications as authenticated by QA International Certification Ltd., UK or International Certifications Ltd., New Zealand. Arch Pharmalabs has submitted Type II DMFs with the following DMF Numbers to the USFDA: 17693, 17954, 17953, 18215, 20444, 19744 and 20681.

Learn More For Corporate Enquiries "H" Wing, 4th Floor, Tex Centre, Off Saki Vihar Road, Chandivali, Andheri (E), Mumbai - 400 072, India. Phone : 91-22-40756789 Fax : 91-22-2847 1234 / 1002 Email : Info@archpharmalabs.com Website : www.archpharmalabs.com For Customers / Vendors Outside North America "H" Wing, 4th Floor, Tex Centre, Off Saki Vihar Road, Chandivali, Andheri (E), Mumbai - 400 072, India. Phone : 91-22-40756705 Fax : 91-22-2847 1234 / 1002 Email : Info@archpharmalabs.com For Business Development / Project Enquiries in North America Mr. Raj Iyer, Ph. D., President Arch Pharmalabs (USA) Inc., 19201 Sonoma Highway, PMB 244, Sonoma, CA 95476. Phone : 707-938-1247 Fax : 707-938-1892 Email : Raj.Iyer@archpharmalabs.com Sitemap | Disclaimer | Privacy Policy Copyright © Arch Pharmalabs 2008. All Rights Reserved. Website Designed and Developed By Phi.