Last Updated on October 2, 2024 by The Health Master
Raipur: A one-day workshop on medical device regulation in India and legal documentation was organized in the auditorium of Sri Sathya Sai Hospital, Atal Nagar Nava Raipur.
This workshop was organized in collaboration with Food and Drug Administration (FDA), Chhattisgarh, and Drug Control Officers (India) Welfare Association (DCOIWA).
Controller, Food and Drug Administration, Chhattisgarh KD Kunjam and State Licensing Authority, Food and Drug Administration, Chhattisgarh Basant Kumar Kaushik were present as chief guests in the program.
Experts from different states were invited to this workshop. Lalit Kr. Goel, Assistant Drug Controller, Food and Drug Administration (FDA), Haryana, gave his presentation on Medical Device Regulation in India, and Rajendra Harna, Assistant Drug Controller (Retd), FDA, Haryana, spoke on Legal Documentation.
In this workshop, assistant drug controllers and drug inspectors (a total of 80 officers) posted in different districts of the state participated in large numbers and answered questions from the experts.
The stage in the program was conducted by Drug Inspector Piyush Jaiswal and Drug Inspector Lakshmi Kaushik.
Drug Control Officers (India) Welfare Association (DCOIWA) is a national organization working for the welfare and education of drug officers, headed by G. Koteshwar Rao, Former Drug Inspector, Telangana, Baldev Chaudhary, Drug Control Officer, Rajasthan is its Secretary.
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After the workshop, the Treasurer of this national organization Parmanand Verma, Drug Inspector, Food and Drug Administration, Chhattisgarh presented a vote of thanks to all the officers and guests for the successful organization of the workshop.
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