Albert

Boylston, Massachusetts

medical product design and development

patent prosecution

patent infringement

infringing product tear-down & evaluation

technical review

claim construction

patent portfolio evaluation and management

Building and leading cross-functional development teams across multiple sites including foreign collaborations

Working with foreign (Asian, European, Israeli) suppliers and co-developers

M&A activities on both buying and selling side of transaction

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Medical device standards & requirements: IEC-60601 (Medical Electrical Equipment), 21 CFR 820 (Quality Systems and Design Controls), IEC-62304 (Medical Device Software), IEC-62366 (Medical Device Usability), 510K's, risk management, ISO-10993 (Biocompatibility), MDD 93/42/EEC (EU regulations)

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