
Proficient in Pre-formulation, Formulation, Research, Production, Packing, and Stability studies
Skilled in conducting Pharmacopeia-standard dosage form evaluations
Well-versed in ICH, GMP, cGMP, and GLP Guidelines for regulatory compliance
Possesses extensive knowledge of site-specific manufacturing processes, enhancing efficiency
Familiar with analytical test methods and various Pharmacopoeias for accurate quality assessments
Sound understanding of Quality Management Systems for maintaining quality standards
Proficient in Production and R&D processes, fostering continuous improvement
VENKATESWARLU.P*, "Formulation and In Vitro Evaluation of Lansoprazole Delayed-Release Capsules," International Journal of Innovative Pharmaceutical Research (IJIPR), Volume 4, Issue 3, Pages 328-336 (2013).