Tulex Pharmaceuticals
Venkat Dharmalingam is an accomplished quality assurance professional with extensive experience in the pharmaceutical industry. Currently serving as Vice President of Quality Assurance at Tulex Pharmaceuticals since January 2020, Venkat manages site quality and compliance, oversees FDA inspections, and directs GMP training for personnel. Prior roles include Senior Director of QA at Tulex Pharmaceuticals Inc., and various positions at Novel Laboratories, Inc., where responsibilities included approving and releasing finished products and handling investigations. Venkat's career began in analytical services at Par Pharmaceutical, and early experiences include roles in quality control and education as a lecturer. Venkat holds a Master’s and Bachelor’s degree in Pharmacy from The Tamilnadu MGR Medical University, India.
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Tulex Pharmaceuticals
Tulex Pharmaceuticals was established in the fall of 2014 as a technology driven specialty pharmaceuticals company led by a team of highly experienced and proven scientists. We are a U.S. based company located in Cranbury, NJ and our focus is on developing and marketing innovative drug products to serve our patients in need. Tulex is a fully integrated pharmaceutical company that has quickly expanded from a Research & Development entity to a fully functional cGMP facility capable of product development, analytical testing, product registration, and commercial manufacturing & packaging of high quality drug products. Tulex plans to commercialize products via strategic partnerships with the U.S. and other major markets.