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Stuart G. Levy, Ph.D.
                                     Principal, SGL Chemistry Consulting

           92 Fairmont St .                                                 (781) 316-2594
           Arlington, MA 02474                                              (617) 504-3519 (cell)
                                                                            Email: [email protected]

           SERVICES OFFERED:

                  Expertise in Chemical Development
                      o   Evaluation and optimization of synthetic routes to drug candidates
                      o   Adaptation of discovery chemistry routes for scale-up
                      o   Chemical process development and optimization
                      o   Creation and execution of fit for purpose R&D, production and cGMP manufacturing strategies and
                         plans
                      o   Design of syntheses of stable isotope and radiolabeled molecules for in vivo studies
                      o   Physicochemical characterization
                      o   Solid state chemistry – polymorphism, salt screening and selection
                      o   Sourcing of raw materials, excipients and standards
                  Vendor Selection, Engagement and Management
                      o   API, drug product, analytical, custom synthesis, QA and regulatory support
                      o   Creation of requests for proposal
                      o   Definition of scope of work, deliverables and timelines
                      o   Facilitation of performance and completion of work
                      o   Technology transfer  - assembly of tech transfer packages, performance of tech transfer to and
                         between vendors and organizations
                      o   Excellent vendor network
                  Problem Solving
                      o   Troubleshooting of chemical process development and API manufacture, drug product process
                         development and manufacture, analytical method development
                      o   Leadership of expert teams in the solution of complex technical problems
                      o   Broad, multidisciplinary consultant network
                  Assistance with Strategy and Management of Drug Development Programs
                      o   Coordination of CMC activities
                      o   Liaison between technical functions, regulatory, QA;  Effective, clear communication across
                         disciplines
                  Technical and Regulatory Documentation
                      o   Drafting, review and editing of development reports
                      o   Authorship, review and editing of CMC regulatory documents, including INDs, NDAs, amendments,
                         biowaivers
                  Regulatory/QA
                      o   Interpretation and application of FDA and ICH guidances pertaining to CMC development activities
                      o   Practical experience in quality audits and mock PAIs in US, India and Japan
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