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DTSTART;TZID=America/New_York:20260922T120000
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SUMMARY:Drug Development Pathways: A Four-Part Webinar Series
DESCRIPTION:Description \n\nDrug development is an interconnected process — scientific\, clinical\, regulatory\, and business decisions made at one stage shape what happens next. \nDrug Development Pathways: A Four-Part Webinar Series provides an accessible\, biotech-specific overview of the complete drug development pathway\, from identifying promising drug candidates through regulatory approval and post-market activities. \nDesigned for professionals who are new to the industry or looking to broaden their understanding\, each 60-minute webinar focuses on a key stage of development\, highlighting the critical inputs required for that phase as well as the strategic outputs passed to the next. \nAttend the complete series for a broader understanding of the drug development lifecycle\, or select the individual webinars most relevant to your role and professional development goals. \nEach live virtual webinar includes an interactive Q&A with the instructor. \n  \nRegistration & Pricing \nBuild your understanding of the drug development lifecycle — one webinar at a time or across the full four-part series. \nParticipants may register for one individual webinar\, a two-webinar bundle\, or the complete four-part series. \nIndividual Webinar \n\nMember Rate: $79\nNon-Member Rate: $99\n\nTwo-Three Webinar Bundle \n\nMember Rate: $149 – $223\nNon-Member Rate: $186 – $280\nUse discount code BUNDLE at checkout to receive bundled rate\n\nFull Four-Webinar Series \n\nMember Rate: $278\nNon-Member Rate: $348\nUse discount code SERIES at checkout to receive bundled rate\n\nWant your organization to gain access to member rates? Email courses@massbioed.org for more information. \n  \nWebinar Schedule \nWebinar 1: Foundations\, Strategy & Candidate Selection\nTuesday\, September 22\, 2026 | 12:00–1:00 PM EDT \nExplore the early drug development process\, including identifying therapeutic targets\, selecting viable drug candidates\, and understanding the regulatory landscape that shapes early development. \nWebinar 2: De-risking & Preclinical Development\nTuesday\, September 29\, 2026 | 12:00–1:00 PM EDT \nLearn how organizations evaluate safety\, establish manufacturing and regulatory strategies\, and prepare successful Investigational New Drug (IND) applications before entering clinical trials. \nWebinar 3: Clinical Trials & Patient Safety\nTuesday\, October 6\, 2026 | 12:00–1:00 PM EDT \nUnderstand the purpose and design of Phases I–III clinical trials\, patient safety monitoring\, pharmacovigilance\, and the role of external vendors in successfully conducting clinical research. \nWebinar 4: Regulatory Approval & the Post-Market Lifecycle\nTuesday\, October 13\, 2026 | 12:00–1:00 PM EDT \nDiscover what happens after successful clinical trials\, including regulatory submissions\, commercialization planning\, post-market surveillance\, and lifecycle management. \n  \nWho Should Attend? \nThis webinar series is designed for professionals who want to better understand how their work fits into the broader drug development lifecycle\, including: \n\nIndividuals transitioning into the life sciences industry\nProfessionals new to biotechnology or pharmaceuticals\nScientists interested in understanding the broader development process\nClinical research professionals\nRegulatory Affairs professionals beginning their careers\nProject managers supporting drug development teams\nBusiness development and commercialization professionals\n\n  \nParticipants Will Learn To \nBy the end of the full series\, participants will be able to: \n\nExplain the major stages of the drug development lifecycle\nUnderstand how scientific\, regulatory\, clinical\, and commercial functions interact\nRecognize key milestones and decision points throughout development\nDescribe the purpose of preclinical studies and clinical trial phases\nUnderstand the regulatory pathway from discovery through commercialization\nRecognize how their specific role fits into and impacts the broader\, interconnected drug development lifecycle\n\n  \nMeet the Instructor \nTonya Pimentel\nPrincipal Consultant\, Pimentel Consulting LLC \nTonya Pimentel is a seasoned leader with 30 years of experience spanning the Cell & Gene Therapy\, Vaccine\, Biotech and Medical Device sectors. A Project Management Professional (PMP) and ASQ Certified Quality Auditor\, Tonya has a proven track record of leading high-stakes initiatives\, including facility startups\, the remediation of quality systems under consent decrees\, and the successful commercialization of complex biologics and gene therapies. As an instructor\, Tonya brings a practical\, “on-the-floor” perspective to Project Management\, focusing on how strategic oversight and cross-functional leadership drive innovation and patient safety in the life sciences. \n  \nQuestions? \nFor questions about the webinar series\, registration options\, or member pricing\, contact courses@massbioed.org.
URL:https://careerhub.massbioed.org/event/drug-development-pathways-a-four-part-webinar-series/
LOCATION:Virtual Event
CATEGORIES:Industry Professionals
ATTACH;FMTTYPE=image/png:https://careerhub.massbioed.org/wp-content/uploads/2026/08/Drug-Development-Webinar-y9mLaR.png
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