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Welcome to Quasaar GmbH

Your reliable partner for pharmaceutical services

Quasaar GmbH stands for many years of experience in quality control, stability and aging studies, GMP analytics, and support in pharmaceutical development. Our commitment to the highest standards of quality, innovation, and efficiency ensures not only strict compliance with all regulatory requirements but also the satisfaction of our clients.

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GMP analytics

    • Quality control of raw materials, excipients, active pharmaceutical ingredients (APIs), and finished medicinal products
    • Batch release (EU retest)
    • Method validation, verification, and transfer
    • Biopharmaceutical studies
    • Human and veterinary sectors
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Contract analytics

    • Development of analytical methods (chromatography – dissolution – particle analysis – titration – wet chemistry)
    • Formulation screening and compatibility testing for product development
    • Biopharmaceutical characterization
    • Specialized analytical methods – special analyses
    • GMP or GSP (Good Scientific Practice)
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Stability studies (GMP)

    • Execution of stability studies (clinical samples, primary stability, and ongoing stability) according to ICH guidelines and aging studies (ASTM)
    • Design and execution of stress studies and forced degradation studies – cyclic storage conditions
    • Storage of large-volume containers (pallets, bags, drums, and bulk materials)
    • Storage studies with narcotics (controlled substances)
    • Preparation of stability protocols and reports
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Consulting

    • Scientific consulting for analytics, biopharmaceutical studies, and product development
    • Consulting for the preparation of GMP documentation and GMP processes
    • Development of qualification and validation concepts
    • Execution of QA tasks and communication with regulatory authorities
    • Consulting on the handling of controlled substances
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GMP outsourcing partner

As a certified outsourcing partner, we offer flexible, efficient, and customized solutions for your operational challenges. We support you in rapidly expanding your capacities when needed and in successfully implementing technically demanding projects.

Our services include:

    • Many years of experience in pharmaceutical quality control and development
    • Extensive capacities for stability studies and storage under various climatic conditions
    • Customer-oriented and stable project teams
    • Flexible support during capacity bottlenecks with low error rates and on-time delivery
    • High responsiveness in project management
    • A trustworthy and reliable partnership
    • QP activities for veterinary and human medicinal products (manufacturing authorization available)

Discover the advantages of partnering with Quasaar and benefit from our expertise and commitment.


Customer Spectrum

Our customer spectrum ranges from globally operating research-based pharmaceutical companies, full-service CMOs, and raw material manufacturers to innovative medium-sized generic companies and research-driven start-ups.

As a GMP-certified and FDA-approved company, we support you throughout the entire product lifecycle — from development to market launch.

What’s new

APV: GMP Basic training Laboratory, 11.11.2025

GMP Certification 2025

CPHI 2025 Frankfurt