Welcome to Teadus Pharma
What We Do
- Chemical Library.
- Identification of hits.
- Lead Identification.
- Lead Characterization.
- Lead Optimization.
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Process Chemistry
- Non-Infringing route .
- QbD-DOE study (CQA and CPP assessment).
- Process Development and Optimization​.
- Process Characterization study (Spike & Purging study, OFAT).
- Pilot Scale Run.
- Impurity Synthesis ​and Characterization.
- Polymorph Study.
- Cutting Edge technologies​.
- Process Engineering​ Assessment (FMEA).
- Process Safety/Hazop Assessment
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Pre-Clinical Supply
- Physicochemical properties
- Milli-gram to g scale API Synthesis for GLP studies
- API process qualification and stability
- Analytical method development and validation
- Impurity profile Identification
- Gram scale API for preliminary formulation studies
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Clinical Supply
- Process Characterization study as per ICH guideline
- Gram to kilo gram scale of NCE/API manufacturing
- KSM / RSM, Advanced intermediate Manufacturing and Supply.
- cGMP manufacturing of NCE / API
- Phase appropriate analytical method validation
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Commercial
- Process Validation
- Multi Ton manufacturing and supply of NCE/APIs in any scale
- Global regulatory agency approved facilities
- Comprehensive quality management systems
- Hassle free shipments to global markets
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Formulation Development
- Oral solids
- Liquids
- Injectables
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Analytical Services
- Method development
- Method validation
- Stability studies as per ICH guideline
- Impurity characterization
- Reference standard qualification
- Force Degradation Study
- Physico-chemical property study
- Extractable & Leachable study
- Excipients/API/FDF samples characterization
- Specific surface area analysis
- Packing material testing
- Osmolality and sub visible particle count (Injectable preparation)
- DVS
- Water activity study
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