Medpace Germany GmbH
Biotechnology, Medical Technology
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Short facts
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- Manufacturer
- Year founded not available
- 1 Employees (site)
- Turnover: <5m EUR
Products/services: A global leader in research-based drug and device development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to drug and device approval. As a therapeutically-focused Clinical Research Organization (CRO), we view ourselves as stewards of your drug and device, leveraging our extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. From addressing the needs of small and midsize biotechnology companies to full-service offerings for global pharmaceutical companies, Medpace has the breadth, depth, and flexibility to deliver a superior result, specific to your needs, on six continents. Clinical Research, Cardiovascular Diseases, Metabolic Diseases, Oncology, Monitoring A global leader in research-based drug and device development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to drug and device approval. As a therapeutically-focused Clinical Research Organization (CRO), we view ourselves as stewards of your drug and device, leveraging our extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. From addressing the needs of small and midsize biotechnology companies to full-service offerings for global pharmaceutical companies, Medpace has… read more
Basic data
Company
Medpace Germany GmbH
Street
Theresienhöhe 30
PC / City
81339 München
County
Upper Bavaria
Phone
+49 89 8955718-0
Fax
0800-184-4276
Homepage
Language skills
English, Japanese
Profile/competences
Core competencies
Medpace, established in 1992, is a full-service Contract Research Organization (CRO), who partners with leading pharmaceutical and biotech organizations to bring promising new drugs to market. Medpace combines comprehensive regulatory consulting with efficient clinical trial management to provide sponsors with exceptional support in drug development. Proven leaders in medical and scientific research monitor every project. Medpace physicians have first-hand experience working with regulatory agencies to successfully guide projects through the complexities of the regulatory process. The medical expertise and regulatory guidance provided by Medpace leads to reduced costs and increased efficiencies for our valued customers.
Key sectors / sub-sectors
- Biotechnology: Contract research (CROs) and contract manufacturing (CMOs)
- Medical Technology: Medical Technology
- Medical Technology: Technical services for medical technology
NACE industries
- Research and experimental development on natural sciences and engineering 72.1
Certifications
not available
Sales markets - target industries
not available
Sales markets - target countries
not available
Cooperation offers
not available