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Phytochemistry, Phytoengineering,Research & Development, Operational Standardization

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  • Patent and Bibliography search combined with Process Development analysis towards definition of Drug Registration strategy.
  • Review of the most updated literature (scientific publications and patents) and industrial insights regarding R&D, manufacturing and quality control (QC) methodologies.
  • Intermediate & Final products Specifications according to Clinical evidence, Feasibility study and Market/Regulation evolutions.
  • Technology & Know-how transfer at all manufacturing processes level (Post-harvest, Drying, Extraction, Refining, Purification, Formulation & Packaging).
  • R&D trials, Experimental Design and Process optimization based on Nomad Labs know-how and Best Practices (valuable industry insights). Coordination between Operations, R&D and QC departments.
  • Development and validation on QC laboratory methodologies for Batch Release according to the relevant Pharmacopeias.
  • Establishing of key partnerships with Academic and private institutions in terms of process development and technology transfer for developing intellectual & industrial property (IP, patents etc). Close cooperation with partners, and scientific project management.
  • Standardization of Operational Procedures (SOP creation) for critical manufacturing steps.
  • Regulatory requirements and strategy for product development & registration.
  • Continuous improvement and innovation (new products & formulations, process intensification & optimization etc.)