Diteba Research Laboratories provides full-service analytical laboratory testing services.  We offer a comprehensive array of cGMP-compliant analytical chemistry services for the analysis of Active Pharmaceutical Ingredients, Inactive Ingredients, In-Process Materials and Finished Goods utilizing the brightest academic ideas and scientific solutions to provide more flexible and R&D-intensive solutions for your drug development needs.  These are:

• Analytical Method Development and Validation
• Analytical Method Transfers from Clients
• Impurity, Metabolite and Degradation Product Identification
• Raw Material Testing (USP/NF, EP, BP, JP)
• Organic Volatile Impurities/Residual Solvent
• Quality Control Release Testing
• Preservative Effectiveness Testing
• Dissolution Testing
• In Vitro Release Rate Studies
• Forced Degradation Studies
• Stability Storage and Testing

Diteba has the flexibility to adopt client-supplied methods, compendial methods or methods that we have developed and validated on behalf of our clients. When using client-supplied analytical methods, we follow a method transfer protocol written by us or our client and approved by the client.  For Compendial methods, these are verified according to a verification protocol.

Diteba's chemists have a broad working knowledge of many dosage forms including solid oral dosage forms (tablets, capsules), semi-solids (creams, lotions, ointments, gels, oral liquids and aerosols), sterile liquid dosage forms and medical devices (coated stents).  We also have a experience working with large or small molecules.