Ms Vanishree Acharya has more than 21 years of work experience. She has worked on training and consulting for Organizations and laboratories in the Life Sciences domain and has vast background in the analytical method development and instrumentation for small molecules acting as building blocks for Pharmaceutical Drug Discovery and pharmaceutical Quality arena conforming to various GMP and GLP requirements. She is widely experienced in the field of chemical, pharmaceutical and Bio-Pharmaceutical support, analysis, instrumentation and training. She is also experienced in preparing and assisting for several GMP, GLP, ISO and FDA audit compliances. As part of the consulting assignments, she has providing inputs to GMP manufacturing, Quality laboratories and Software Development groups for activities related to the Regulatory Compliances.