A Leading global pharmaceutical Contract Research Organization

Drug formulation development services

Our drug formulation development services include partition coefficient determination, dissolution rate, solubility studies in various solvent systems, excipient compatibility studies, pre-formulation drug characterization services, and solubility optimization. Our degradation studies include acid, base, heat, oxidation and photostability assessments under accelerated and long-term conditions.

SP Formulations develops customized dosage forms for your desired route of administration.  We offer drug formulation development services from simple toxicology screening to final clinical dosage forms. Our in-house expertise is able to satisfy your formulation needs through tailored programs using a systematic approach in solving difficult issues such as, deliverability, solubility, stability, etc.  SP Formulations is knowledgeable in developing parenteral, oral, topical and ophthalmic formulations in a wide variety of dosing forms, including liquid and semi-solid.

Drug formulation development services:

  • Partition coefficient
  • Solubility studies in solvent systems
  • Drug/excipient interactions
  • Degradation studies (acid, base, heat, photostability, oxidation
  • Solubility optimization
  • Excipient selection and screening
  • Formulation and evaluation of a wide variety of dosage forms
  • Physical and chemical stability
  • Compatibility of storage materials
  • Dissolution testing
  • Tox formulations to clinical formulations
  • Preservative efficacy testing
  • Scalability
  • GLP pre-clinical production services
  • cGMP clinical production and labeling services