I am a Regulatory Affair Expert, having 9 years of experience in Drug Regulatory affairs.
My highest qualification Master in Pharmacy with majors in Pharmaceutical Analysis and Quality Assurance.
I have been involved in various regulatory activities ranging from Drug development to the life cycle management at global level. I am experienced in managing regulatory activities in markets specifically Europe, South Africa, Australia, WHO, US and few other semi regulated countries.
My professional strength is managing CMC activities for Medicinal Products, while looking for regulatory compliance and guiding inter and intra department for regulatory advice during product development....