Yogesh D. Sadhale, PhD
Director, Pharmaceutical Development
Yogesh manages all aspects of personnel and operations related to formulating and manufacturing a client’s pharmaceutical materials for Phase I, II and III clinical trials., Yogesh is responsible for scale up and validation of clinical trial materials, and manufacturing and packaging clinical trial batches under Current Good Manufacturing Practices (cGMP) guidelines. In addition, Yogesh provides planning and budgeting for pharmaceutical development operations, and hires, trains and manages pharmaceutical development staff.
With 20 years of experience in the pharmaceutical industry, Yogesh previously worked at Patheon Manufacturing Services, where he managed pharmaceutics and process development. He holds a doctorate in pharmaceutical sciences from the Medical University of South Carolina. Connect with Yogesh on LinkedIn