We deliver analytical services on:
Active pharmaceutical ingredients (API)
Raw materials
Excipients
Solid formulations
Tablets (coated and uncoated)
Capsules (hard and soft gelatin capsules)
Liquid formulations (solutions, suspensions, injectables)
Semi-solid formulations (gels, creams, ointments, suppositories)
Our services include but are not limited to:
Analysis according to official monographs (Ph Eur, USP, AOCS)
Method development/implementation/optimization & validation
Stability studies
Cleaning method development and validation
Forced degradation studies
Impurity profiles
Structural elucidation of unknowns
Reference standard characterization
Solubility studies
Response factor studies
Residual solvent analysis
Batch control
Release analysis
Process support
Technology transfer to QA at contract manufacturing partner
QP – Qualified person service
Patent infringement – analytical support
FDA dietary supplements consulting
Contact us to find out how Vitas can contribute in releasing your medicinal product.