Sanatrack

I lead CMC development programs for small molecules and peptides, via the oral, topical and (intra)-ocular administration route for start-up and small biotech companies.

As pharmacist with a Ph.D. in formulation and a QP certification, and with experience ranging from early development to commercial manufacturing, I have a strong knowledge of product development, quality, and regulations which I can leverage to drive pharmaceutical product development and production.

I manage the product development activities with suppliers, including DS manufacture, formulation & process development, analytical validation, in vitro, ex vivo and in vivo testing, clinical supply plans and preparation of IMPD. I drive vendor selection and qualification, budget preparation, implementation and oversight.