Mr. Tirumal Rao has over 22 years of work experience in the Biotech healthcare industry. He has overall experience in Analytical R&D /QC leader, CMC and Virology, global technology transfer to GMP production plants and their market authorization related to biosimilars, viral and genetic engineered vectors. He worked for Biosimilar projects (few are successfully commercially launched in India, Europe, US) GCSF,PEG/GCSF, GM-CSF, Erythropoietin, Ranibizumab,Natalizumab, Liraglutide,Simhagluite ,Denosumab, Trastuzumab, Adalimumab, Ustekinumab, Bevacizumab and Rituximab & Infliximab).