Leonard Eisner

Committee Member Tc 210 Wg2 Gen Asp Fr Appl of Qlty Princ Med Dvcs @Iso - International Organization For Standardization

Portland, OR, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Apr 2023 — Present

Committee Member Tc 210 Wg2 Gen Asp Fr Appl of Qlty Princ Med Dvcs @Iso - International Organization For Standardization

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General aspects stemming from the application of quality principles to medical devices

EDUCATION

1989 — 1993

Santa Clara University

Master of Business Administration - MBA, Business Administration and Management, General

1980 — 1985

San José State University

BSEE, Electrical Engineering

SKILLS

IsoCmdrFdaRegulatory Strategy DevelopmentProduct CertificationInternal Auditing Medical Device Quality SystemsStandardization21 CfrIso 13485Iec 60601Product DevelopmentCmdcasU.s. Food and Drug Administration (Fda)Quality SystemQuality SystemsRegulatory RequirementsTestingRegulatory DocumentationRegulatory SubmissionsFda GmpStandards DevelopmentStandards ComplianceEuQuality System ComplianceIec 60601-1 Series of StandardsCe MarkingCenelecCross-Functional Team LeadershipSupplier QualityIso 14971MddEuropean UnionMedical DevicesIso 9000Technical FilesMedical Device DirectiveFda Quality System RegulationRegulationsInternational StandardsQuality Management

ABOUT LEONARD EISNER

I am the founder and principal compliance and regulatory consultant of Eisner Safety Consultants, we provide the medical device industry with product safety compliance & regulatory support.I ensure my clients’ medical device compliance needs are met with uncompromising attention to detail and quality. I provide my clients with practical assessments of their product(s) and provide strategies & support to help them through the medical device product compliance maze.As an expert in the standards development process, I have been staying at the forefront of evolving medical device standards for over 20 years with standards such as the IEC 60601 series, ISO 15223, ISO 204171. Provided expertise to 100’s of SMEs and Fortune 500 companies for successful medical device compliance projects2. Reviewed/generated 30+ product safety and labeling/marking sections of EU technical file/technical documentation (MDD/MDR)/ DHF for active medical devices and active medical implantables3. Expert Member of development teams on IEC 60601-1, edition 3.2 (via IEC TC62/SC 62A/MT28 & MT30 & WG14 & IEC TC62A/Ad Hoc Group 62••••••01) and 4th edition of IEC 60601-1 - Working Groups assignments in process currently - https://bit.ly/IEC60601-1FourthEdTimeToGetInvolvedIsNOW

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