Surendra Kumar Shrivastava Email and Phone Number

To resolve all issues related to pharma regulatory, analytical, production, product development and other related matters

Quality Control, Quality Assurance, Validations, Formulation Developments and Documentation are some of the Industrial experiences. Generated documents related to MFR, BMR, BPR, SOPs, Site master file, Quality Manual, Quality policy, Deviations, change controls, Facing the regulatory audits, conducting training on SOPs cGMP, Audits reports and CAPA Preparation. Well exposed to all QA functions like cGMP, Quality issues. Handled the outsourcing third party Manufacturing sites, conducting the corporate audits and a fair knowledge in Regulatory Affairs.Well exposed to all the formulations like Tablets, Capsules, Dry syrups, Liquid orals; Dry powders sterile preparations, Liquid sterile preparations, Nutraceuticals, Ayurvedic formulations.Conducting Stability studies both real time and accelerated as per ICH guidelines