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Sridhar Reddy

Sridhar Reddy

Sridhar holds post graduate degree in Pharmacy, having 23 years of experience in Sterile and Non Sterile manufacturing facilities with acquaintance to various domains of pharmaceutical industry. Has strong pharma background with in-depth knowledge, in implementation of Quality System Management to ensure that “Quality is built into the process” and in handling Site Quality Management in different pharma companies.

Expert in handling Projects of different molecules, including sourcing of vendors for Materials, conducting vendor Audits, ANDA submissions and launching of products at commercial scale in US & European market for Injectable and solid oral dosage forms.

Successfully handled regulatory Audits of US-FDA, UK-MHRA, EU, ANVISA-Brazil for both Sterile and Non Sterile manufacturing facilities.

At Life Pharma, Sridhar is responsible for overall Quality functions, implementation of systems & procedures and Representative of site for QA systems.