Who we are

PharmaLex India is the Indian arm of the PharmaLex Group. PharmaLex India offers great value to global customers through its flexible offshore business delivery models. Our offerings span around;

  • End-to-end regulatory services, customized to meet client requirements with the capability of delivering on a global and local level.
  • End-to-end PV support services including on ground support (Local QPPV/LSR).
  • Development Consulting and Scientific Affairs to assist with optimal strategy on your product development.
  • Our customers have a Pharmaceuticals/Biotechnology/Consumer Care/Cosmetics and Medical Devices industry background.
  • Our teams are qualified medical professionals or PhD’s with over 20 years of life science industry experience.
  • Our subject matter experts are able to offer cost-effective solutions to customers worldwide and work in close cooperation with global teams and customer project stake holders.

Local Contact

  • Rashim Sharma
    Assistant Director, Business Development and Marketing PharmaLex India 3rd Floor, Plot No. 1 and 2,
    Tower A, Maple Corporate Park,
    Sector – 125,
    Noida,
    Uttar Pradesh – 201301
    +91 120 5178478/79/80
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What our clients say about us

We are working with a number of large pharma companies and are looking to create a consortium of partners to collect feedback on expertise, availability and outcomes. If you would be interested in joining our consortium, please contact us on contact@pharmalex.com.

  • They are available when we need to talk to them despite any time zone differentials

    Japan based medium sized company
    Manager

  • Thanks so much for your support over the past 30 days. Your commitment and timely communication have made working with you all a pleasant experience.

    US Biotech
    Senior QA Associate

  • Pharmalex provided the resources we needed to compile Investigational Medicinal Product Dossiers for our biological products. The dossiers were delivered on time with the trusted quality we expected

    Small US Biopharmaceutical Company
    Sr Director Regulatory Affairs CMC

  • Provided honest feedback and collaborative working solutions to obstacles

    South Korea based medium sized company
    Manager

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