Analytical Development

At Adragos, we specialize in analytical development, offering a suite of services tailored to the pharmaceutical sector. Our state-of-the-art laboratories are equipped with the latest instrumentation, ensuring all analyses meet the stringent EU-GMP standards and ICH guidelines. Whether you need independent analytical testing or an integrated development package, our expertise guarantees precision, quality, and compliance.

Analytical Development Services

• Method development and validation
• Forced degradation
• Dissolution studies
• Chemical analysis of APIs
• Finished product controls
• Process validation controls
• ICH stability, photostability and in-use stability
• Transfer of analytical methods
• Drug product release (EU QP)

Technologies

• Empower® Chromatography Data System
• Liquid chromatography (PDA, RID, or UV)
• Ultra-Performance Liquid Chromatography (UPLC)
• Ion Exchange Chromatography (IEC)
• Liquid Chromatography–Mass Spectrometry (LC MS)
• Gas Chromatography (GC) for Headspace or liquid injections (ECD and FID)
• UV spectrophotometry
• Dissolution testing (USP I, II & III)
• Walk-in stability rooms and stability chambers
• Photo stability chamber
• Differential scanning calorimetry
• Optical microscopy

Tailored Analytical Solutions

We understand the critical role of analytical services in drug development. Our laboratories deliver a broad range of analytical capabilities designed to address specific client requirements effectively. Every service adheres to rigorous quality controls and regulatory standards, providing reliable support for pharmaceutical innovation.

Validation and Support Services

Enhancing drug formulation and development, our analytical services team leverages advanced technology and deep scientific knowledge to offer robust validation of analytical methods. This comprehensive support ensures that all procedures meet global regulatory expectations and help streamline the path to market for new pharmaceutical products.

Certification and Compliance Assurance

Our facility and processes comply with all relevant GMP standards, including rigorous operational and performance qualifications annually. We also uphold the highest standards for computerized systems and data integrity, ensuring that our services meet all regulatory and quality benchmarks.

Flexible Analytical Service Options

We provide exceptional analytical services for pharmaceutical development. Our commitment to excellence in analytical development ensures that we deliver superior quality and compliance in all aspects of pharmaceutical testing and development.

We offer Clinical Development in Athens, Greece

With more than 3,000 sqm of R&D facilities, Adragos Athens specialises in the development of Value Added Medicines and has been recently upgraded with HPAPI capabilities.

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