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Project Descriptions 4
  • On behalf of various U.S. and foreign biopharmaceutical manufacturers, located facilities with the appropriate capabilities for the preparation, process development, or commercial manufacture of: (1) a recombinant protein from E. coli for therapeutic use; (2) a recombinant monoclonal antibody; (3) a generic antibiotic; (4) a recombinant virus produced in human cell culture; (5) a recombinant protein from E. coli used for nutritional purposes; (6) a recombinant protein used as a pharmaceutical adjunct; and (7) a relatively large volume of a low molecular weight specialty chemical.  The assignments required varying degrees of involvement, but always encompassed providing a short list of possible facilities and an analysis of the strengths and weaknesses of the different facilities and staffs.
  • Discussion with a major European chemical company with interests in biotechnology revealed a complementarity between their interests and those of a mid-size American company, which the European company had approached unsuccessfully.  Based on my acquaintance with senior management and an analysis of the benefits of working together, a meeting was arranged at which the two groups discussed their mutual interests.
  • A biotechnology company is developing a process for production of a specialty chemical by fermentation followed by chemical manipulation of the intermediate to yield the final product.  Many process options exist, and the client requested a cost analysis using preliminary data to serve as the basis for making some predictions of final product cost as well as to focus development efforts on the favorable routes.
  • An evaluation was undertaken of the fermentation and downstream processing technology at a foreign manufacturer of pharmaceutical products.  The aim was to identify competitive strengths and weaknesses and to assist the company in increasing its manufacturing productivity for a number of processes.  As a result of our involvement, strain improvement programs were successfully implemented,  and some significant process improvements were made.

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