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Regulatory Information & Facilitation Center

Regulatory Information & Facilitation Center

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Tag: Clinical Affairs

R Clinic on Planning Regulatory Pathway & Essential Requirements for Medical Devices & IVDs for the Indian Market

June 30, 2023Events

R Clinic on Planning Regulatory […]

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R Clinic on Designing Clinical Trials for Medical Devices & Biopharmaceutical Products

December 21, 2022Events

R Clinic on Designing Clinical […]

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R Clinic on Clinical Study Design for Medical Devices & Diagnostics

April 27, 2022Events

R Clinic on Clinical Study […]

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  • Internship Program
    • Exploring EU MDR and its demand in India. Finding out the potential leads for EU MDR 2017/745 services
  • Requirements/preferences
    • Students pursuing B.Pharm / M.Pharm with interest in Regulatory Affairs
    • Basic knowledge of EU MDR and CE marking preferred.
    • Familiarity with market research methods- online surveys, data analysis, and reading industry reports.
    • Familiarity with MS Office tools.
    • Strong communication skills

Click Here To Apply

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