Manish Anand

Biography

Mr. Anand has many years of experience in the biopharmaceutical industry including responsibility for interactions with international regulatory agencies including the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). Mr. Anand has been involved in the development of drugs, biologics, blood products and vaccine therapies for a diverse range of therapeutic areas such as hematology, oncology, CNS, inflammation and orphan disease. Prior to joining Symic Bio, Mr. Anand was Director of Regulatory Affairs at Portola Pharmaceuticals. Mr. Anand has also served in regulatory affairs positions at BioMarin, Vanda, MacuSight and Medimmune. Mr. Anand received a M.S. in Biotechnology from the Johns Hopkins University and a B.S. in Chemistry from Lafayette College.

Research Interest

Development of drugs, biologics, blood products and vaccine therapies for a diverse range of therapeutic areas such as hematology, oncology, CNS, inflammation and orphan disease.