Attorney at Law
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Lisa A. Mammel
Lisa A. Mammel, Attorney at Law provides specialized legal advice and counseling to life science companies in the areas of research, clinical development, regulatory approval, intellectual property protection, and commercialization of health care products.
Lisa established her solo legal practice in 2004, after practicing in the Life Sciences Practice Group at Cooley Godward LLP (now Cooley LLP) for several years. In setting up her own firm, Lisa chose to concentrate on the area of clinical trials. By focusing on this practice area, Lisa provides clients with a considerable depth of expertise with regard to the regulatory, legal, and ethical issues affecting clinical research.
Lisa works with various clients in the life sciences community, among them, biotechnology companies, pharmaceutical and medical device manufacturers, contract research organizations, and academic institutions. Lisa’s understanding of legal and regulatory issues is complemented by her appreciation of companies’ needs for cost-effectiveness and efficiency. She effectively drafts and negotiates clinical research agreements, as well as counsels clients on compliance matters.
Life sciences companies have increasingly engaged foreign-based sites in their clinical trial research. Lisa's earlier career in international diplomacy and her language fluencies are assets in this regard. She successfully negotiates agreements among the various stakeholders, with the knowledge of the applicable foreign and U.S. regulations, as well as with an appreciation of how practices differ among the international parties.
Lisa established her solo legal practice in 2004, after practicing in the Life Sciences Practice Group at Cooley Godward LLP (now Cooley LLP) for several years. In setting up her own firm, Lisa chose to concentrate on the area of clinical trials. By focusing on this practice area, Lisa provides clients with a considerable depth of expertise with regard to the regulatory, legal, and ethical issues affecting clinical research.
Lisa works with various clients in the life sciences community, among them, biotechnology companies, pharmaceutical and medical device manufacturers, contract research organizations, and academic institutions. Lisa’s understanding of legal and regulatory issues is complemented by her appreciation of companies’ needs for cost-effectiveness and efficiency. She effectively drafts and negotiates clinical research agreements, as well as counsels clients on compliance matters.
Life sciences companies have increasingly engaged foreign-based sites in their clinical trial research. Lisa's earlier career in international diplomacy and her language fluencies are assets in this regard. She successfully negotiates agreements among the various stakeholders, with the knowledge of the applicable foreign and U.S. regulations, as well as with an appreciation of how practices differ among the international parties.
Lisa A. Mammel
Attorney at Law
Lisa@LMammeLaw.com
Attorney at Law
Lisa@LMammeLaw.com