Ardena

Navigating you through drug development

General Information
Company Name
Ardena
Founded Year
2017
Location (Offices)
Belgium +5
Founders / Decision Makers
Number of Employees
466
Industries
Health Care, Pharmaceutical
Funding Stage
-
Social Media

Ardena - Company Profile

Ardena is a pharmaceutical Contract Development and Manufacturing Organization (CDMO) that offers a comprehensive suite of services to guide companies through the drug discovery and development process. With a headquarter in Ghent, Belgium, Ardena operates facilities in the Netherlands, Sweden, and Latvia, catering to a global customer base across the Health Care and Pharmaceutical industries. Since its establishment in 1994, Ardena has been committed to supporting clients in creating effective and compliant drug substances and products for clinical trials. The company's integrated service offering encompasses solid-state chemistry, API and nanomedicines development and manufacturing, analytical and formulation development, drug product manufacturing, bioanalytical, drug discovery, and dossier development services. Ardena's approach involves a detailed planning phase for each project, allowing for staggered investments and risk mitigation at every stage of the drug development process. One of Ardena's key strengths lies in its dossier-centric approach, ensuring compliance with regulatory standards and facilitating the compilation of regulatory dossiers in a timely and cost-efficient manner. This approach aligns with the company's overarching goal of expedited drug development and delivery to patients. With a focus on streamlining the development process, Ardena's multidisciplinary team is dedicated to driving projects forward by leveraging its integrated offering. The company's client base ranges from emerging biotech firms to tier-one pharmaceutical companies, highlighting its versatility and ability to cater to diverse needs within the industry. In summary, Ardena's emphasis on integrated services, meticulous planning, regulatory compliance, and expedited drug development sets it apart as a valuable partner for companies navigating the complex journey from molecule to clinic.

Taxonomy: Pharmaceutical CDMO, Drug development, API & nanomedicines, Analytical & formulation development, Bioanalytical, Regulatory compliance, GMP Manufacturing, Clinical logistics, Solid state research, Contract Development & Manufacturing Organization, Drug Product, Drug Substance, Regulatory dossier development, Pharmaceutical services, Multidisciplinary team

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