The current program is offered with inputs from the USP Education system. The program is designed to upgrade the knowledge & Skills of the participant from the healthcare industries to realize Quality Goals. The program provides an overview to learn quality management systems, documentation, data management, Physical, chemical, and wet chemical analysis, Instrumental analysis, and Quality Control of input materials as well as finished products. It is expected, on completion, the participants will have an understanding of the Quality Goals of the Pharmaceutical Industry, and engage them to learn and implement the knowledge in day to day working.
This program is intended for professionals working in industries, researchers, and students from wide range of backgrounds. The aim is to develop their knowledge, skill, and competence pertaining to quality management system in pharmaceutical industries. The course in designed to provide fundamental and practical skills to the persons working in the pharmaceutical industries to ensure that each prepared medicine reaching a patient is safe, effective and of acceptable quality. This comprehensive program includes both technical and managerial activities of the quality management systems of industries which include evaluation of product, documentation, data integrity, performance and reviewing quality control lab tests, process etc. The managerial activities include selection of reliable suppliers, preparing contract terms, monitoring their performance, and performing inspection procedures throughout the distribution network.
The building of quality culture in the industry provides the information on role and responsibilities of personnel, basic elements of quality management like infrastructure or “quality system”, encompassing the organizational structure, procedures, processes resources and systematize actions necessary to ensure adequate confidence that a product (or service) will satisfy given requirements for quality. The syllabus is designed by experts from Industry keeping the global perspective. The program is subdivided into courses and modules which are articulated through four quadrants approach, using Multimedia, demonstrations, virtual labs, Self-instructional materials, e books, having illustrations, case studies, open-source contents etc. In addition, the Discussion forms are established to seek clarifications. Continuous assessments are held through assignments seeking short or long answers for Questions.
Any graduate in science (B.Sc./ BE / B.Tech / MBBS / BDS / B.Pharm / M.Pharm ) from any recognized Institution / University
Industry Professionals like Working Chemists, Executives, Managers, Group Leaders, Heads of QA / QC / Production in Pharmaceutical Industry or Academicians are also eligible to apply for this course.
.INR 40000 for Indian Nationals
USD 600 ( Equivalent in INR would be charged )
My objective is to work innovatively to advance my career, profession and for betterment of the institution.
Dr Anand Kumar Tengli is presently working as Assistant Professor in the Department of Pharmaceutical Chemistry. In his more than 15 years of teaching and research experience, he has published more than 25 scientific papers in peer reviewed national and international journals. He has attended national and international conferences to present his research findings. He has guided 12 PG students and presently guiding 03 PG students. He is member of various professional national and international organizations.
Impurity Profiling of Drugs, separation, spectral chracterisation & evaluation of toxicity studies of impurities
Analytical &bioanalytical method development
Synthesis and Biological Evaluation of Heterocyclic compounds