At Adragos Pharma, we offer a wide variety of pharmaceutical services ranging from formulation and analytical expertise to pilot scale and commercial production and packaging for sterile and non-sterile liquids, solids, and semi-solids.
Our experts can help you process all your pre-formulation and formulation needs. They will design all the necessary steps to validate the manufacturing process, API quality and choice of excipients. We also offer a broad selection of primary and secondary packaging.
Our teams of analytical experts offer extensive services that include the following:
Study of active ingredients
Development and validation of analytical methods for drug products, raw materials, and cleaning methods
Development and validation of dissolution profiles
PROCESS DEVELOPMENT AND OPTIMIZATION
In our facilities, we can manufacture batches for clinical testing, incl. high-potency products of the following dosage forms:
Sterile and non-sterile liquids
TECHNICAL TRANSFER AND VALIDATION
Our highly experienced, multidisciplinary transfer teams on site will support your product transfer in close cooperation with your project team. Thereby, our teams manage the transfer project holistically incl. pilot charges, scale-up, analytics, stability testing, and process validation.
Every Adragos Pharma site is equipped to perform in-house analytics and stability testing and thus is able to design, execute and analyze pre-stability, regulatory or commercial stability studies, according to the International Council on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) conditions.