Our Services
Discover Our Services
Within our range of CDMO services, we offer Visual Inspection to assist our clients in adhering to various regulations. We utilise cutting-edge technology to guarantee that our clients’ products conform to the rigorous standards of the market.
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Innovative, secure, and compliant packaging solutions customised for our clients’ diverse product range are another of our specialised CDMO services.
Handling controlled drugs requires precision, security, and regulatory knowledge. As part of our comprehensive CDMO services, our facilities in Kawagoe, Greece, and Livron offer specialised solutions to manage these essential yet stringent requirements.
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Our out licensing model provides partners with access to our Generic and Value Added Medicines products, helping expand product ranges, enter new markets, and accelerate healthcare solutions.
Efficient and reliable supply chains are crucial to the pharmaceutical industry. Our strategic locations allow us to offer optimised supply chain and planning services, ensuring timely delivery across markets.
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Our CDMO services extend to comprehensive release and recurrent testing that includes method establishment, raw material testing, in-process chemistry testing, API and drug product release testing, ICH stability testing, and comparator testing.
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Effective cold chain management is essential for maintaining the quality of temperature-sensitive pharmaceuticals. Our facilities offer comprehensive solutions, guaranteeing the secure and regulatory-compliant handling of our clients products throughout the entire process.
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Our support can help our clients navigate the complex landscape of pharmaceutical regulations. From consultation and submission strategy to compiling the dossier, submission, and follow-up until the grant of Marketing Authorization (MA) and post-approval.
Frequently Asked Questions
What are CDMO services?
CDMO services (Contract Development and Manufacturing Organization) provide pharmaceutical companies with comprehensive support, covering both drug development and manufacturing. These services include activities like formulation development, clinical trial manufacturing, commercial-scale production, packaging, supply chain management, stability testing, and regulatory support, allowing companies to bring their products to market efficiently and cost-effectively.
How can Adragos Pharma’s CDMO services support my pharmaceutical product from development to market?
Our CDMO services provide comprehensive support from drug development to commercialization. This includes visual inspection, pharmaceutical packaging, supply chain planning, and regulatory support. We offer tailored solutions, ensuring your product meets the highest standards for quality, safety, and regulatory compliance across each stage of its lifecycle.
What benefits does your supply chain planning service offer to pharmaceutical companies?
Our supply chain planning services optimize logistics by leveraging our strategically located facilities. This ensures efficient delivery, inventory management, and cost reduction, ultimately accelerating your product’s path to market and enhancing supply chain reliability.
How does your visual inspection service help maintain product quality and regulatory compliance?
Our visual inspection service uses advanced technology to ensure that products meet stringent quality and regulatory standards. This process helps identify any inconsistencies or defects, ensuring compliance and safeguarding the product’s market reputation.
How can Adragos Pharma support my product’s compliance with market regulations through packaging?
Our pharmaceutical packaging services offer secure, compliant, and customized solutions tailored to your product’s needs. We ensure that packaging meets market-specific regulatory standards while maintaining product integrity, which is crucial for product success in global markets.
What makes Adragos Pharma a reliable partner for handling high potency APIs (HPAPIs) and controlled substances?
We have dedicated facilities, such as our Athens site for HPAPI synthesis and specialized sites in Kawagoe, Greece, and Livron for controlled substances. Our experience in handling these complex products ensures precision, safety, and compliance with strict regulatory guidelines, making us a trusted partner for managing high potency and controlled drugs.
