Get to the clinic faster with Adare Pharma Solutions
In early stage pharma development, getting to clinical trials fast is key. Unlike other companies that lack the in-house skill to make that happen, Adare is your go-to CDMO for speed, expertise, and proof-of-concept data. Our experienced scientists and experts provide hands-on insight, always with scalability in mind. We’re not just quick…we’re flexible, adaptable, and innovative.
We offer comprehensive development services, from preformulation to scale-up, that build a solid foundation for successful proof-of-concept studies. We’re experts in developing oral dose formulations for tablets, capsules, suspensions, and minitabs, and we can provide pediatric, modified release, taste masked, and patient-centric formulations.
With integrated end-to-end CDMO services that ensure a seamless transition to manufacturing, Adare is with you from start to finish.
Comprehensive Preformulation Capabilities
- Physicochemical characterization
- pH-dependent solubility profile
- Solubility profile in solvents (aqueous, non-aqueous and buffered fluids)
- pKa and Log P
- Particle size and shape
- Microscopy (SEM, polarized microscope, etc)
- Flowability, bulk/tap density
- pH-dependent solubility profile
- Solid state characterization
- Crystal forms
- Hygroscopicity
- DSC, DVS and PXRD (outsourced)
- Solid state stability (heat/humidity and light)
- Crystal forms
- Solution stability (pH, oxidation, heat and light)
Development & Validation of Analytical Methodology
- Formulation support
- On-Site GMP testing of API, excipients, and finished product
- On-Site GMP testing of API, excipients, and finished product
- Physical characterization
- Controlled substance handling: Schedules I-V
- Clinical supplies testing
- Method transfer
- Analytical Method Development & Validation
- Chromatography, Dissolution, and Monograph techniques
- Phase-appropriate method validation
- USP/NF, ASTM, EP, BP, JP and CP
- Chromatography, Dissolution, and Monograph techniques
- Onsite Stability & Storage
- Full ICH stability storage capabilities and stability testing
- Large capacity stability storage and testing under ICH-controlled conditions
- 25°C, 60% RH; 30°C, 65% RH; 40°C, 75% RH
- 25°C, 60% RH; 30°C, 65% RH; 40°C, 75% RH
- ICH-compliant photostability studies
- Full ICH stability storage capabilities and stability testing
- Abuse-Deterrent Testing
- Stability-indicating impurity methods
Speak With An Expert
Armando Pedoto
Senior Vice President, Italy Operations
Armando Pedoto is the Senior Vice President, Italy Operations at Adare Pharma Solutions, where he oversees manufacturing, R&D operations and strategic initiatives across Adare’s Italian sites. With over 20 years of pharmaceutical industry experience, Armando has held various leadership roles, including Vice President of Global Procurement & Supply Chain and Italy Manufacturing Operations at Adare.
Prior to joining Adare, he served as Chief Operating Officer at Doppel Farmaceutici and held quality management positions at Mipharm and Pharmacia Italia. Armando’s expertise spans manufacturing, operational excellence, quality control and assurance, regulatory affairs, procurement and supply chain management, and ESG .
He holds a master degree in Chemistry and Pharmaceutical Technologies from the Università degli Studi di Milano and brings a wealth of knowledge and leadership to Adare’s global operations.