At Xedev, we accelerate your product development journey by combining extensive formulation expertise, advanced process development, and state-of-the-art manufacturing capacity.

We pride ourselves on being more than a service provider – we operate as an extension of your team. With communication, transparency, and scientific excellence at the core of our approach, we ensure a seamless and productive partnership.

Ready to strengthen your development pipeline?

Our values, mission and culture

Mission

Our mission is to remain fully committed to delivering innovative technologies and high-quality service solutions that support our customers throughout their drug product development journey. By combining deep scientific expertise with a flexible and responsive mindset, we help accelerate timelines and strengthen confident, data-driven decision-making. 

About Xedev – team discussion on pharmaceutical development
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About Xedev – company values driving pharmaceutical development
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Values

Our company values – symbolized by the colors in our logo – represent the principles that guide every interaction, decision, and project at Xedev. They stand for:

Trust • Loyalty • Perseverance • Confidence • Stability • Harmony • Growth • Ambition • Nature • Enthusiasm • Creativity • Success • Health • Happiness • Fascination

These values reflect the foundation of who we are and how we work: with integrity, curiosity, and dedication to long-term partnerships.

Culture

At Xedev, our culture is defined by expertise, precision, responsiveness, and genuine partnership.

Experts in formulation and process development

Our multidisciplinary team brings deep scientific experience, enabling us to solve complex challenges and design robust, scalable solutions.

We specialize in small-scale process development that provides fast, reliable insights before going into larger-scale manufacturing.

We adapt to your project’s needs, offering agility and clear communication to keep your development moving forward without delays.

We support early-stage molecules and prepare them for PK, Tox, and clinical studies, ensuring a smooth transition toward clinical success.

At Xedev, you are never a number. We prioritize personal communication, tailored solutions, and close collaborations – we are part of your team!

About Xedev – expert team collaborating on formulation and manufacturing
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We are proud to house a team of skilled, committed, respectful, and well-balanced professionals who strengthen one another through collaboration and shared purposes. Working within a state-of-the-art facility with a strong sustainability score, our team combines scientific expertise with responsible innovation to deliver outstanding results for our customers.

Our services

Drug product development

We specialize in formulation and process development for solid drug products. Using our deep scientific expertise, we design customed and scalable solutions to meet the requirements of each customer.

Our analytical capabilities support your program from early formulation screening through clinical manufacturing.

Start your formulation and process development project with us.

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About Xedev – operators working in GMP cleanroom manufacturing area
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Drug product manufacturing

Xedev provides R&D and GMP batch manufacturing services, supporting PK, Tox, Phase I and II clinical studies. Our flexible production capabilities range from small-scale to large-scale batches, ensuring the right fit for your development phase and material needs.

History

Procept, founded in 1994 and backed by more than 30 years of experience, is the pioneer and specialist in small- and pilot-scale processing equipment. By enabling development with minimal material use and precise data logging, Procept technologies allow customers to design, optimize and scale their processes with confidence – resulting in one of the fastest tracks from concept to market.

About Xedev – scientists working with laboratory instruments
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About Xedev – Xedev branding on lab coat inside laboratory environment
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Xedev was established from the Procept process equipment demo center, where rising global demand for outsourced formulation and process development services led to the official launch of Xedev in 2012.

Since then, Xedev has evolved from a small feasibility laboratory into a specialized, knowledge-driven CDMO with strong capabilities in formulation development, process development and manufacturing for the pharmaceutical, biotechnology, chemical and food industries.

Xedev shares its facility with Procept, creating a unique and powerful synergy. Xedev integrates Procept’s advanced technologies into its services, while Procept engineers deliver immediate technical support. This bi-directional collaboration accelerates innovation, improves efficiency, and strengthens the quality of all Xedev operations.

In addition to the Procept equipment, Xedev offers complementary technologies – including analytics and tableting – to support complete drug product development workflows.

With this integrated setup and global customer reach, Xedev combines scientific excellence, state-of-the-art equipment, and rapid development capabilities – supporting clients from early-stage feasibility through clinical success.

Want to discover how our integrated approach can benefit your project?

About Xedev – Xedev branding on flag
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Leadership team

Filip Van der Gucht, CEO at Xedev

Filip Van der Gucht

CEO
Russel Pescod, CFO at Xedev

Russel Pescod

CFO
Lieselotte De Smet, CSO at Xedev

Lieselotte De Smet

CSO
Natascha Van Vooren, QA Manager at Xedev

Natascha Van Vooren

QA Manager
Veerle Timmerman, Head of Production at Xedev

Veerle Timmerman

Head of Production
Laurien Goossens, QC Manager at Xedev

Laurien Goossens

QC Manager
Elien De Coninck, Project Manager at Xedev

Elien De Coninck

R&D Manager
Joana Macedo, Project Manager at Xedev

Joana Macedo

Project Manager
Lise Vandevivere, Business Developer & Project Manager at Xedev

Lise Vandevivere

Business Developer & Project Manager

Certifications

Certificate of GMP Compliance of a Manu­facturer

Xedev is certified for Human investigational medicinal products in accordance with Eudralex Volume 4 Good Manufacturing Practices (GMP) and Reg (EU) 536/2014.

Looking for a CDMO partner who understands your vision and drives your success from early development through clinical supply?