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Avrio

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
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