<p dir="ltr" style="line-height: 1.38; margin-top: 12pt; margin-bottom: 12pt;">[size= 11pt; font-family: Arial,sans-serif; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap]The [/size][size= 11pt; font-family: Arial,sans-serif; color: #1155cc; background-color: transparent; font-weight: bold; font-style: normal; font-variant: normal; text-decoration: underline; -webkit-text-decoration-skip: none; text-decoration-skip-ink: none; vertical-align: baseline; white-space: pre-wrap]MD-42 license[/size][size= 11pt; font-family: Arial,sans-serif; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap] is a crucial legal permit issued by the State Licensing Authority under CDSCO for businesses that want to legally stock, sell, or distribute medical devices in India. This is a must-have for wholesalers and retailers, and the application process, which uses Form MD-41 on the SUGAM portal, can be complex. I'm starting this thread to ask for your insights and share experiences with the MD-42 application. What documents did you find most challenging to prepare? Are there any specific tips for a smooth online submission or dealing with the inspection? Let's help each other streamline the process and ensure full compliance.[/size]