Awareness of the Current Regulatory Requirements for Medical Products and Clinical Trials in India [22nd Feb 2019]

Introduction:
This event is an R Clinic organized by BRBC. The goal is to understand regulatory requirements and roadmap for securing regulatory approval for medical products in India. The Clinic will also focus on understanding the relevant Acts/ Laws/ Rules and standards applicable to the respective drugs and medical devices.

This Clinic will be useful for innovators and startups in the following medical device categories: Clinical grade screening, diagnostic and recording instruments | Medical devices for clinical intervention or treatment |Surgical tools and aids | Assistive devices or disability aids or image reconstruction or artificial body parts | Molecular in vitro diagnostics | Topical, surface and open wound contact products or products in body orifices | Implants made from polymers, body tissues, metal, plastic, ceramic etc| Sensors, IOT, Big Data, Mobile, Cloud, AI/ML, Analytics, decision support, software etc used for making medical decisions | Supplies & consumables used in diagnostics, preservation, hospital equipment | Recreational and popular diagnostics, wearable.

When: 22nd Feb 2019
Where: Seminar Hall, 1st Floor, PSG Institute of Medical Sciences & Research

Limited seats!!! Total number of seats: 50
No Registration Fee Required

Preference: Startup companies (LLC/PLC) vs. individuals if we receive more than 50 applications || Organizers reserve the right to select participants so as to optimize the group for better interaction and ensure benefit to as many startups as possible. NOTE: Registration closes once 50 seats are full or on xx Feb 2019(whichever comes sooner).

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