Eesha Vyas
Regulatory Affairs Associate@ GSK
London, Greater London, United Kingdom
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Eesha Vyas is a highly experienced professional with 14.1 years of work experience in medical research, laboratory, clinical trials, medical writing, and gene therapy. Currently, she is working on the R&D Regulatory Affairs 'Future Leaders Programme' at GSK in London. Prior to this, she held positions at Therpeutic Groups, where she owned the HIV centralised Product Tivicay. Eesha has also worked at GRA-Labelling, where she was responsible for the HIV portfolio of products. She is currently pursuing an MAA for a novel Gene Therapy product within CMC.
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@gskbio.com
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About

I am currently on the R&D Regulatory Affairs 'Future Leaders Programme' at GSK. This is a two year graduate programme with rotations in various regulatory disciplines. Till date, I have worked within the Therpeutic Groups, taking ownership of the HIV centralised Product Tivicay for its registration in the EMAP region. My second rotation was in GRA-Labelling where I was responsbile for the HIV portfolio of products, including three Centralised and one Mutual Recognition Product, Retrovir. I am now working towards the EU registration and approval of an MAA for a novel Gene Therapy product within CMC.

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Work Experience

980 Great West Road, Brentford, Middlesex, TW8 9GS, GB

Pharmaceutical Manufacturing

103019
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Eesha Vyas's Professional Milestones

  • Regulatory Affairs Associate (2014-09-01~2016-09-01): Maintained compliance with international regulations, mitigating risks and ensuring adherence to regulatory requirements.
  • Customer Consultant (2010-08-01~2013-08-01): Provided personalized insights to clients, improving their overall customer experience and satisfaction.
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Education

英国伦敦大学学院
英国伦敦大学学院

Msc Cell & Gene Therapy

1325376000-1356998400
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