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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