Harikrishna Reddy B

A focused professional with over 4.6 years of rich experience with the Pharma Industry,Resourceful in reviewing the technical specifications as well as other quality documents in adherence to various quality management systems,Excellence in monitoring and maintaining quality system as per cGMP requirements and provided appropriate guidance and ensuring cleanliness of the workplace & laboratory as per GLP,Review of Exhibit batch documents (including but not limited to) ascertain their adequacy forfiling -BMRs, MPRs, Specifications / STPs & CoAs, Stability protocol & data,Responsible for ensuring the software complies with the requirements set forth in the FDA guideline 21 CFR Part 11