FORMULATION DEVELOPMENT

Avrio’s cGMP facility incorporates state-of-the art equipment and a dynamic team of experienced formulation scientists with a successful track record to provide clients cutting-edge solutions and responsive customer care.

Our formulation team consists of highly skilled, experienced scientists with a comprehensive understanding of all facets of the drug development process and dosage forms with a stellar track record of preformulation and formulation development.

In-depth Pre-formulation Services

Solubility and pH-rate Profile
Log D/Log P
Excipient Compatibility
Stability Evaluation
pKa determination
Polymorph Screening
Purity Determination
Hygroscopicity Studies
Physicochemical characterization
Particle Size Distribution
Intrinsic Dissolution

Comprehensive Formulation Services

Parenteral Dosage Forms
Solid, Semisolid and Liquid Dosage Forms
Lyophilization Cycle Development
Ophthalmics
Hospital Products
Emulsions/Suspensions
Liposome and Microsphere Encapsulation
Admixture and Container/Closure Compatibility Studies
Pilot Batch Production and Stability Analysis
Toxicology Supply Manufacturing/Dosing Solutions

Disciplined Technology Transfer

Procedures and Processes

Batch Record Development
Method Transfer, Development and Validation
Scale-up Studies