Drug Product
Analytical & Bioanalytical Services
Contract Research Organization
Regulatory, Tech Transfer & Support Services
Company Overview
About
Nuvisan is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in Biologics Manufacturing, Monoclonal Antibodies, Vaccines
Therapeutic Areas
Infectious Disease
Quick Facts
HQ:France
Founded:2019
Employees:149
Capabilities & Services
Core Capabilities
- Small Molecule API
- Small Molecule Drug Product
- Oral Solid Dose
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Oral Solid Dose
Containment Capabilities
Cytotoxic / ADC Handling
Production Scales
Pilot Scale
Phase I Clinical Trials
Clinical
Markets Served
North America
Manufacturing Facilities
3 sites worldwide
NUVISAN GmbH
Im Wirrigen, Waltrop, 45731
Site Capabilities
1 capabilityANALYSIS
NUVISAN GmbH
Robert-Koch-Allee 29, Gauting
NUVISAN GmbH
Wegenerstrasse 13, Neu-Ulm, 89231
Site Capabilities
1 capabilityANALYSIS
International Regulatory
EU GMP Certificates
6
Regulatory Bodies
EMA/EudraGMDP
Regulatory Approvals
Drug Approval E506AX
Health Canada · #APR-32B6YBBI · 2019-09-01
Drug Approval F5TVO3
FDA · #APR-WVCP32AI · 2021-09-01
Case Studies
0 published case studies showcasing past projects, challenges and outcomes.
Certifications
EMA GMP Certificate
European Medicines Agency
Cert #: CERT-YQ4K8F0Y
Issued: 2020-05-17
Expires: 2025-01-18
ISO 9001:2015
International Organization for Standardization
Cert #: CERT-LPLJ9OYL
Issued: 2020-10-22
Expires: 2025-01-21
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Key facts about Nuvisan
- Nuvisan is headquartered in France.
- Nuvisan was founded in 2019.
- Nuvisan has 149 employees.
- Nuvisan has 3 manufacturing sites listed on CDMO Hub, in Waltrop, Germany, Gauting, Germany and Neu-Ulm, Germany.
- Nuvisan's capabilities include Small Molecule API, Small Molecule Drug Product and Oral Solid Dose.
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