Ph.D.-M.B.A. Educated Life Sciences Writer and Editor. I Write Business Plans, Grant Proposals and Produce FDA Medical Device, Pharmaceuticals, and Biologicals Submissions. I have a background in biomedical, pharmaceuticals and biologics R&D, medical data bioanalytics and personalized medicine, quality assurance & regulatory compliance, and I was on the team that gained US marketing approval for Taxol for anticancer and Orencia for rheumatoid arthritis. I also obtained FDA-cleared device registration for Pathway Genomics Corporation and EU...
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Feb 12, 2014|Article Writing|Private|Completed
Nov 12, 2013|Article Writing|Private|Completed
Jun 18, 2012|Academic Writing|Private|Completed
Sep 13, 2011|Grant Writing|Private|Completed
I Provide Writing & Editing in the Life Sciences. This includes Articles and Reviews, eBooks, Print Books, Market Research Reports, Marketing Plans, Business Plans, Grants Development, and Biomedical Quality and Regulatory Compliance Documents Writing & Submission to Regulatory Bodies Worldwide.
I have a Ph.D. in Cell & Molecular Biology, and Biochemistry; a M.S. in Microbiology; a B.S. in Biological Sciences with a Chemistry Minor; and a M.B.A.
I Have 29 Years of Experience in the Health Care/Life Sciences Area. Expert in Writing/Editing R&D Proposals, Grant Proposals, Market Research Reports, Marketing Plans, and Business Plans.
Authority on Medical Products Technical, Regulatory and Quality Documents Preparation and Management.
Experienced in Writing Pharmaceuticals, Medical Device, Biologics, Stem Cell and Combination Medical Products, Biotechnology, and Environmental Sciences Reports and White Papers.
Expertise in Grant Writing: SBIR and STTR Grants and Contracts, Federal Contracts, BioDefense Grants, and Private Foundations Grants.
Also Experienced in Writing Life Sciences Articles and eBooks, Providing Website Content, and Summarizing Highly Technical Information for Marketing/Sales Campaigns and for the General Public.
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