Pharmaceutical Testing
Scientific Analysis Supporting Product Quality And Development
OUR PRE CLINICAL SERVICES
Pharmaceutical Testing
Explore the latest scientific insights, research advancements, industry developments, and regulatory updates from Ribosome Research Centre. the use of the method for agreed testing purposes.
Pharmaceutical Testing Services Scope
Analytical Method Development- Analytical Method Verification/Validation As Per ICH And USP Guidelines
- Extractable And Leachable Study As Per USP And PQRI Guideline
- Nitrosamine, NDSRIs And Other Genotoxic Impurities Analysis
- Excipient Compatibility Studies
- Structural Characterization of API and Excipients
- Bioanalytical Method Development and Validation
- Cleaning Validation
- Elemental Impurities Analysis as per ICH
- Assay, Impurity Profiling and Residual Solvents analysis
- Assay of Heparin, Enoxaparin and Streptokinase
- Molecular Weight Distribution Analysis with Size Exclusion Chromatography
- Physical and Chemical Evaluation of Various API and Formulations
- Composition of ions by Ion chromatography
- Stability Studies as per ICH Guidelines
Our Process
Our Approach To Accurate &
Compliant Testing
Build your career in a research environment that values scientific curiosity, quality and teamwork. At Ribosome Research Centre, people
contribute to work that supports the understanding of products and the evidence behind development decisions.
Requirement Understanding
We begin by understanding your product, testing requirements, and regulatory objectives to define a clear analytical strategy.
Method Development & Planning
Our team develops and optimizes analytical methods, ensuring alignment with ICH, USP, and global regulatory standards.
Testing & Analysis
Samples are tested using advanced instrumentation such as LC-MS/MS, ICP-MS, and other validated techniques for accurate results.
Reporting & Compliance Support
We deliver detailed, audit-ready reports and provide support for regulatory submissions and compliance requirements.
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