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Gilberto Dalmaso has over 35 years’ experience in pharmaceutical microbiology and sterility assurance. During his distinguished career he led a series of technology-driven process improvements using scientific methods, while achieving GMP compliance and regulatory approvals mainly for aseptic processes and sterile products.

Today Gilberto is the Global Pharma Advisor and Subject Matters Expert for GDM Pharma Consulting. In this role he collaborates and consults with global pharmaceutical companies to develop and implement science-based strategies and processes that utilize Quality by Design (QbD) principles to monitor, control, and improve the chemical, physical, and microbiological state of various production processes.

Having contributed significantly to industry leaders such as Lonza, Qiagen, Roosterbio, Emergent Biosolutions, and CBMG, Alex brings a blend of technical acumen with hands-on expertise. As a career QC scientist and growing compliance expert, she has consistently demonstrated a commitment to operational excellence and continuous improvement.

Alex holds an undergraduate degree in Biochemical Engineering from UMBC and a graduate degree in Biomedical Engineering from Clemson University. Beyond the laboratory, she brings a global perspective, having lived abroad in China, and is fluent in Mandarin Chinese. Alex also enjoys rock climbing and indulges in tabletop gaming.

Abby Roth, founder of Pure Microbiology, has been supporting the testing and consulting needs of the pharmaceutical, medical device, and compounding industries since 2004. Her background in pharmaceutical microbiology includes extensive knowledge of environmental monitoring.
Abby served as a USP Compounding EC member during the 2015-2020 cycle.

She is an involved member of the Controlled Environment Testing Association (CETA), serving on the Board of Directors, speaking at its annual meetings, and chairing committees for the revision of five CETA Application Guides. Abby has been invited to speak for state boards of pharmacy and for national organizations.

Having contributed significantly to industry leaders such as Lonza, Qiagen, Roosterbio, Emergent Biosolutions, and CBMG, Alex brings a blend of technical acumen with hands-on expertise. As a career QC scientist and growing compliance expert, she has consistently demonstrated a commitment to operational excellence and continuous improvement.

Alex holds an undergraduate degree in Biochemical Engineering from UMBC and a graduate degree in Biomedical Engineering from Clemson University. Beyond the laboratory, she brings a global perspective, having lived abroad in China, and is fluent in Mandarin Chinese. Alex also enjoys rock climbing and indulges in tabletop gaming.

Vanessa Figueroa leverages her combined knowledge of the Pharmaceutical, Biotechnology and Medical Decives industries to provide manufacturers across the US, Europe and India with critical laboratory operations management and personnel training programs to ensure compliance with cGMPs as well as global regulatory standards.

Combining hands-on Quality Control, Sterility, Inspection, and Compliant Operations with an educational leadership approach and natural business acumen, Vanessa brings 17+ years of real-time experience to deliver transformational real-world results.

Vanessa Figueroa leverages her combined knowledge of the Pharmaceutical, Biotechnology and Medical Decives industries to provide manufacturers across the US, Europe and India with critical laboratory operations management and personnel training programs to ensure compliance with cGMPs as well as global regulatory standards.

Combining hands-on Quality Control, Sterility, Inspection, and Compliant Operations with an educational leadership approach and natural business acumen, Vanessa brings 17+ years of real-time experience to deliver transformational real-world results.

Having contributed significantly to industry leaders such as Lonza, Qiagen, Roosterbio, Emergent Biosolutions, and CBMG, Alex brings a blend of technical acumen with hands-on expertise. As a career QC scientist and growing compliance expert, she has consistently demonstrated a commitment to operational excellence and continuous improvement.

Alex holds an undergraduate degree in Biochemical Engineering from UMBC and a graduate degree in Biomedical Engineering from Clemson University. Beyond the laboratory, she brings a global perspective, having lived abroad in China, and is fluent in Mandarin Chinese. Alex also enjoys rock climbing and indulges in tabletop gaming.

Vanessa Figueroa aprovecha su conocimiento combinado de las industrias farmacéutica, biotecnológica y de dispositivos médicos para ofrecer a los fabricantes en Estados Unidos, Europa e India programas críticos de gestión de operaciones de laboratorio y capacitación de personal para garantizar el cumplimiento de las Buenas Prácticas de Manufactura (cGMP) y las normas regulatorias globales.

Combinando el control de calidad práctico, la esterilidad, la inspección y las operaciones conformes con un enfoque de liderazgo educativo y un agudo sentido de los negocios, Vanessa aporta más de 17 años de experiencia en el sector.

Enric Adserà has a degree in Chemistry, Chemical Engineering and MBA from ESADE. Since 2018 he works in Tiselab as Project Manager of SherpaPharma providing his experience and knowledge in the application of Environmental Monitoring solutions in the pharmaceutical industry.

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Enric Adserà es Licenciado en Químicas, Ingeniería Química y MBA por ESADE. Desde 2018 trabaja en Tiselab como Project Manager de SherpaPharma  aportando su experiencia y conocimientos en la aplicación de soluciones de Monitorización Ambiental en el sector farmacéutico.

Santi studied telecommunications engineering and an MBA. Since 2005 he works at Tiselab, where he has helped to consolidate the current team, achieving sustained growth, and diversifying the company into various divisions. In 2016, he started the SherpaPharma project after realizing that pharmaceutical companies had an opportunity for significant improvement in Environmental Monitoring.

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Santi estudió ingeniería de telecomunicaciones y un MBA. Desde 2005 trabaja en Tiselab, donde ha ayudado a consolidar el equipo actual, consiguiendo un crecimiento sostenido y diversificando la compañía en varias divisiones. En 2016 inició el proyecto SherpaPharma al ver que en las compañías farmacéuticas había una oportunidad de mejora importante en la Monitorización Ambiental.

Enric Adserà has a degree in Chemistry, Chemical Engineering and MBA from ESADE. Since 2018 he works in Tiselab as Project Manager of SherpaPharma providing his experience and knowledge in the application of Environmental Monitoring solutions in the pharmaceutical industry.

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Enric Adserà es Licenciado en Químicas, Ingeniería Química y MBA por ESADE. Desde 2018 trabaja en Tiselab como Project Manager de SherpaPharma  aportando su experiencia y conocimientos en la aplicación de soluciones de Monitorización Ambiental en el sector farmacéutico.