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To better assist you with your request, please choose a research area provided by Seda Pharma Development Services Ltd. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.
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Drug Formulation
Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
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Chemistry, Manufacturing and Controls (CMC)
Request Chemistry, Manufacturing and Controls services
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Chemical Stability
Measure the stability of small molecules in solution.
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Bioequivalence Studies
Assess the expected biological equivalence of two proprietary preparations of a drug.
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API Physical Characteristics
Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
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Dissolution Profiling
Measure release of API from formulation (tablet or capsules) under GMP guidelines.
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Excipient Compatibility
Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
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Small Molecule Drug Development Consulting
Request consulting services related to small molecule development.
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API/ Excipients Compatibility Studies
Delineate real and possible interactions between potential formulation excipients and the API as an important risk reduction exercise early in formulation development.
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Chemistry, Manufacturing and Controls (CMC) Consulting
Consultant services related to the development of pharmaceutical and biopharmaceutical drug products that are consistently effective, safe and high quality for consumers.
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