Diploma in Regulatory affairs online course will provideanfundamental knowledge on various practices (viz., GMP, Quality related aspects) documentation requirements, laws and regulations for the manufacture of pharmaceuticals, the regulatory requirements for life cycle management of pharmaceuticals.
At completion of the course, it is expected that students will be able tounderstand
Any graduates pursuing in the field of Pharmaceutical Sciences, Medical Sciences, Veterinary Sciences, Biotechnology, Microbiology and Life Sciences from any recognized institution.
INR 40,000/- per Year for Indian Nationals
USD 600 per Year ( Equivalent in INR would be charged)
Designation: Associate Professor
Email Id: email@example.com
Qualification: B. Pharma, M. Pharma, Ph.D
No of Publication: 63
To become regulatory affair professional in pharmaceuticals and also to establish regulatory centre for dossier compilation consultant
Dr. G.N.K.Ganesh is an assistant professor and Course Coordinator department of pharmaceutical regulatory afffairs. His research focuses on self multiparticulate drug delivery system nano drug delivery system for the past one decade including nanoemulgel for topical application. To his credit he has 01 patents filed under Intellectual property of India for minitablets punch fabrication. Published research articles in reputed journals viz., Journal of Pharmaceutical Investigation, Journal of Bioequivalence and Bioavailability, Asian Journal Pharmaceutics to name some. He is interested in developing targeted drug delivery system which helps in the recrudescence cancer. He is currently involved in peptide based drug delivery system. Currently he is involved in regulatory science
Pharmaceutical Regulatory Affairs 'Data integrity, Life cycle management, impurity profiling'
Targeted drug delivery system
Tumor homing peptides