Our Directors
Profile of Mr. D Gopal Krishna
Mr. Gopal Krishna aged about 54 years is the Director of the Company. He is a post-graduation science student who worked in Dr. Reddys Laboratories in different functions,
He worked for 20 Years in Dr. Reddy’s Laboratories having vast experience in different functions & departments.
He played a critical role in Documentation, Validations, Audits & Compliance, facing Customer Audits (National & International Audits), Departmental Audits such as WHO, CGMP, ISO, USFDA, EDMF, JDMF, TG etc., and supporting in filing the DMF’s to Regulatory Affairs.
For carrier development he selected to Quality Management in Department Manufacturing Excellence, and played a significant role in harmonizing the Manufacturing CORE Standard Operating Procedures across the Dr. Reddys Laboratories units and played a role in development and harmonizing the CORE Quality Assurance Standard Operating Procedures across the DRL.
As a job rotation he shifted to Department Technology & Process Development (T&P), here he worked in association with Chemical engineers in the DRL Units in regarding Solvent Management system for re-cycle & re-use, new products Implementation in Pilot Scale & Commercialization in the Plant Scale, Trouble Shooting and Process Regularization.
Mr. D. Gopal Krishna is a Promotor & Director of Asstrica Laboratories Pvt Ltd. a Active Pharmaceutical industry He run the company for 5 years and made the company sustainable by getting Departmental certifications such as cGMP, ISO, WHO, CDSCO, DCA, and International certifications CEP, Japan and other Muti Level company customer Audits
Profile of Ch. Ganeshwara Rao
His expertise as a Head of Quality Assurance has successfully completed Regulatory Inspections (USFDA, EDQM, Health Canada), ANVISA, COPFERRIS, Domestic customer Audits, CDSCO, DCA, Local WHO GMP Audits and ISO Audits.
He is a Quality Assurance professional, experienced working in Various MNC Active Pharmaceutical Organizations, he has technical and interpersonal skills. Confident and poised in interactions with individuals at all levels. Detail oriented and resourceful in completing multi task projects effectively.
He played a critical role in execution of Product Process Validations, Product Cleaning Validations, Technology Transfers, Documentation, Quality Management Systems, Audits & Compliance and supporting in filing the DMF’s to Regulatory Affairs.
Being a Quality Assurance person he has sound knowledge in both GMP & Regulatory Procedures.
