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.)
