Transo Pharm Germany
Pharmaceuticals, 216 Hazeltine Cir, Siek, Pennsylvania, 19422, United States, 11-50 Employees
Phone Number: +16*********
Who is TRANSO-PHARM GERMANY
Founded in 1987 and based in Germany, Transo-Pharm has established a global reputation as a trusted supplier of active pharmaceutical ingredients (APIs). Via its head office in Siek, Germ...
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- Headquarters: 216 Hazeltine Cir, Siek, Pennsylvania, 19422, United States
- Date Founded: 1987
- Employees: 11-50
- Revenue: $1 Million to $5 Million
- Active Tech Stack: See technologies
Industry: Pharmaceuticals
SIC Code: 5169
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Frequently Asked Questions Regarding Transo-Pharm Germany
Answer: Transo-Pharm Germany's headquarters are located at 216 Hazeltine Cir, Siek, Pennsylvania, 19422, United States
Answer: Transo-Pharm Germany's phone number is +16*********
Answer: Transo-Pharm Germany's official website is https://transopharm.com
Answer: Transo-Pharm Germany's revenue is $1 Million to $5 Million
Answer: Transo-Pharm Germany's SIC: 5169
Answer: Transo-Pharm Germany has 11-50 employees
Answer: Transo-Pharm Germany is in Pharmaceuticals
Answer: Transo-Pharm Germany contact info: Phone number: +16********* Website: https://transopharm.com
Answer: Founded in 1987 and based in Germany, Transo-Pharm has established a global reputation as a trusted supplier of active pharmaceutical ingredients (APIs). Via its head office in Siek, Germany, and regional offices in Asia, USA and India, Transo-Pharm connects suppliers, customers and markets through communication, marketing expertise and mastery of logistics. Transo-Pharm is a fully licensed and certified distributor dealing in pharmaceutical components for the health and veterinary industries. The company has achieved sustainable growth through long term partnerships and ability to deliver flexible, authentic and qualified solutions for pharmaceutical applications. Transo-Pharms expertise for APIs has been developed in close cooperation with the pharmaceutical industry. Professional skills allow the company to provide a customized and complete regulatory support in the areas of qualification of manufactured APIs, GMP consulting and DMF establishment.
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