Ardena Email Formats

Pharmaceutical Manufacturing • Kleimoer 4, Ghent, Belgium • 501-1000 Employees

Ardena Email Formats

Ardena uses 4 email formats. The most common is {first name}.{last name} (e.g., john.doe@ardena.com), used 62.2% of the time.

Format	Example	Percentage
{first name}.{last name}	john.doe@ardena.com	62.2%
{first initial}.{last name}	j.doe@ardena.com	30.3%
{first initial}.{second initial}{last name}	j.odoe@ardena.com	3.1%
{first initial}.{second initial}	j.o@ardena.com	2.1%

Key Contact at Ardena

Dave Seghers

Head of Sales Pharm Division

Mobile @ardena.com

Company overview

Headquarters	Kleimoer 4, Ghent, 9030, BE
Phone number	+3292676510
Website	ardena.com
NAICS	3254
SIC	283
Keywords	API, CRO, Bioanalytics, Pharma, Gmp Manufacturing, Formulation Development, Cdmo, Drug Substance, Solid State Research, Clinical Logistics, Drug Product, Nanomedicines, Pharmaceutical Company, Regulatory & Scientific Writing, Contract Development & Manufacturing Organization
Founded	2017
Employees	501-1000
Socials

About Ardena

We are a global provider of drug development and discovery services, encompassing drug substance, drug product, bioanalysis, and CMC regulatory services across small molecules, large molecules, and nanomedicines. Our six international locations offer comprehensive CDMO and BioAnalytical CRO services to a wide range of clients worldwide. We recognize the intricate challenges associated with advancing a promising molecule from the laboratory to the patient. Our multidisciplinary team is eager to collaborate with you throughout your development process, utilizing specialized technologies to optimize formulation and manufacturing. We possess extensive expertise in spray drying, hot melt extrusion, and lipid-based formulations that enhance bioavailability and solubility. Additionally, our capabilities include polymeric, metal, and lipid nanoparticles for advanced drug delivery applications, as well as high-potency and controlled substance handling for highly specialized therapeutics. At Ardena, all work adheres to the appropriate regulatory standards as you progress through the clinical development pathway. Please contact us to further discuss your clinical and scientific objectives and explore how we can work together.