Discover innovative solutions to the key challenges of the drug safety industry
Milbhor D' Silva | Vice President, Product Safety & Pharmacovigilance Astellas Pharma Global Development
Milbhor D’Silva is a transplant and multiorgan procurement surgeon by background. His clinical work was complemented by live animal research using solid organ models of transplantation. His pharmaceutical medicine career spans 14 years. Over this period he has worked with both, therapeutic drug development (Novartis, Abbott) and medical diagnostic imaging companies (GE-Healthcare-Medical Diagnostics) in both Europe and the US. His work has focused in supporting pre- and postmarketing projects, while working with Health Authorities. Of note, his work in the field of Xenotransplantation with Novartis allowed him the opportunity to engage with the FDA, CDC, WHO, and the UK health authority in the area of planning to mitigate risks following retroviral disease transmission through solid xenografting in humans. Milbhor D’Silva currently leads the Product Safety & Pharmacovigilance group in Astellas Pharma Global Development at Deerfield, IL. Outside of the pharmaceutical field, Milbhor’s interests allow him to be engaged in the work done by the Southern Poverty Law Center in the areas of fighting hate, teaching tolerance, and seeking justice.
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Appearances at this years' conference:
Day one AM - Wednesday 18th April 2012
@ 11.45
Panel Session: The existing harmonisation practices are not working, how can we do this better?
• Is it possible to achieve global harmonisation of safety
regulations and practices?
› Milbhor D' Silva, Vice President, Product Safety & Pharmacovigilance, Astellas Pharma Global Development
Day Two - Thursday 19th April 2012
@ 11.45
Panel session: The future of post authorisation safety- where are we heading?
› Milbhor D' Silva, Vice President, Product Safety & Pharmacovigilance, Astellas Pharma Global Development