Quasaar GmbH

Bringing together expertise, efficiency, and innovation

Since its founding in 2015, Quasaar GmbH has established itself as a reliable and competent partner for the pharmaceutical, medical device, and life sciences industries. We are distinguished by our profound expertise and commitment to delivering innovative solutions that meet the demanding requirements of our clients.

Our team consists of qualified professionals who apply state-of-the-art technologies and strict GMP standards to ensure that every project is executed precisely and efficiently. We take pride in not only providing services but also in guiding our clients throughout the entire development and production process, working together to create solutions that secure the long-term success of their products.

With extensive capacities for stability studies and tailored outsourcing concepts, we offer flexible and scalable solutions that are customized to the specific needs of our clients. Our approach is characterized by a deep understanding of industry challenges and a strong focus on process optimization and increasing efficiency.

We test the latest technologies in real-world practice, adapt them to the relevant regulatory environment, and implement them in daily operations.

The sustainable development and expansion of a highly qualified team is both our primary goal and our key to success. We provide a working environment that fosters innovation and social responsibility. A well-balanced ratio between operations and overhead, combined with short communication paths, enables us to respond quickly and act flexibly in day-to-day business.

Company Profile

Name: Quasaar GmbH

Address: Lichtenkopfer Weg 1, D-66450 Bexbach, Germany

Founded: 02/2015 (HRB 102208), independent company

Business Area: Contract Laboratory (GMP)

DUNS number: 313388660

FEI number: 3014297892

Certifications: GMP-certified, FDA-approved

Manufacturing Authorization (TAM): DE_SL_01_MIA_2023_0009

Our history

  • 02-2024

    5th GMP certification (Bexbach)

  • 06-2022

    Expansion of the stability center

  • 02-2022

    4th GMP audit (Bexbach)

  • 02-2022

    Relocation to Bexbach & expansion of laboratory capacities

  • 11-2020

    3rd GMP audit (Überherrn)

  • 05-2019

    FDA approval (Überherrn)

  • 11-2017

    GMP certification (Überherrn)

  • 10-2015

    First GMP certification (Überherrn)

  • 06-2015

    Operational launch of the Überherrn site

  • 02-2015

    Founding of Quasaar GmbH

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Modern outsourcing concept, fair pricing

We act as your central point of contact and coordinator for all your outsourcing needs. During the project initiation phase, we identify your specific requirements and assemble an optimal service package tailored to your needs. We handle transport logistics, documentation, the establishment of new technologies or method transfers, and the qualification of necessary subcontractors. Our primary goal is to establish a stable and long-term cooperation based on partnership. You define the requirements regarding error rates, responsiveness, and adherence to deadlines.

We test the latest technologies in practical applications, adapt them to the relevant regulatory environment, and implement them into daily operations.

The sustainable development and expansion of a highly qualified team is both our primary objective and the key to our success. We offer a working environment characterized by a high degree of innovation and strong social responsibility. A well-balanced ratio between operations and overhead, combined with short communication paths, enables us to achieve impressive responsiveness and flexibility in day-to-day business.

Pricing model for analytical services

Quasaar offers a customized service and a customer-oriented pricing strategy based on a differentiated hourly rate model.
For GSP projects, the reduced documentation effort is directly passed on to the client as a cost saving.

Pricing model for stability and storage studies

Cost calculation is based on volume units (liters per month).
Costs are adjusted on a regressive basis according to the study plan and the actual stored volumes.
Volume discounts are prospectively factored in based on the maximum annual volume.

Contingent orders

Storage contingents (reserved storage volume) as well as laboratory capacities (reserved FTEs – Full-Time Equivalents) can be contracted on an annual basis and flexibly called upon as needed.