Ivan Toscano Email & Phone Number

- Development of the propitiatory VeraTag technology on assay optimization, pathology assessment, analytical validation, clinical validation and commercial launch of clinical tests in the CLIA-certified, CAP-accredited specialty laboratory. - Provide clinical insight and strategic direction for clinical study collaborations.- Establish relationship with principal investigators/KOLs of leading academic centers and pharmaceutical companies in the US and internationally.- Generate… Show more - Development of the propitiatory VeraTag technology on assay optimization, pathology assessment, analytical validation, clinical validation and commercial launch of clinical tests in the CLIA-certified, CAP-accredited specialty laboratory. - Provide clinical insight and strategic direction for clinical study collaborations.- Establish relationship with principal investigators/KOLs of leading academic centers and pharmaceutical companies in the US and internationally.- Generate medical and scientific information materials; develop and execute publication plan; author and review scientific publications, including abstracts, posters, manuscripts and whitepapers. Show less

- Served as Laboratory Director for the CLIA-certified, CAP-accredited specialty laboratory that specialized in Extreme Drug Resistance (ERD) testing. - Provided pathology services and supervision on high-complexity cancer testing (IHC, FISH, Flow, and PCR). - Oversaw laboratory activities including participation in developing, revising and adhering to all medical and technical policies and procedures affecting laboratory personnel and test performance. - Reviewed and approved SOPs… Show more - Served as Laboratory Director for the CLIA-certified, CAP-accredited specialty laboratory that specialized in Extreme Drug Resistance (ERD) testing. - Provided pathology services and supervision on high-complexity cancer testing (IHC, FISH, Flow, and PCR). - Oversaw laboratory activities including participation in developing, revising and adhering to all medical and technical policies and procedures affecting laboratory personnel and test performance. - Reviewed and approved SOPs related to all high-complexity tests offered by the lab.- Provided guidance for reimbursement optimization.- Evaluated, planed and managed supply and equipment needs and purchases. Responsible for the selection and acquisition of capital equipment. Led and directed maintenance of service facilities, equipment, supplies and area, and assured compliance with established standards and regulatory requirements. Show less

- Development and validation of high-complexity cancer testing (IHC, FISH, Flow, PCR and residual cell detection) in collaboration with many major pharmaceutical companies.- Provided strategic and scientific input to the overall product development plans for projects related to diagnostic needs (phase I to phase II cancer trials) of pharmaceutical companies.- Reviewed and approved SOPs in the lab; adhering to all medical and technical policies and procedures in accordance with GLP… Show more - Development and validation of high-complexity cancer testing (IHC, FISH, Flow, PCR and residual cell detection) in collaboration with many major pharmaceutical companies.- Provided strategic and scientific input to the overall product development plans for projects related to diagnostic needs (phase I to phase II cancer trials) of pharmaceutical companies.- Reviewed and approved SOPs in the lab; adhering to all medical and technical policies and procedures in accordance with GLP practice.- Participated in data analysis and result presentation with pharmaceutical company clients in preparation of pharma client’s product presentation/submission to the regulatory agencies (e.g. FDA). Show less

Bachelor'S Degree, Clinical Medicine, Oncology

Doctor Of Philosophy (Ph.D.), Pharmaceutical Chemistry