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 Smartworks Corporate Park
    Maple Corporate Tower A and B
    Sector-125
    Noida
    Uttar Pradesh 201303
    India

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.

  • 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
  • Our project team were very impressed with the quality of the research and the reports that you sent through. We didn’t need any convincing that your recommendations should be followed. It showed PharmaLex in a very positive light, and the Project Team are keen to work with you again.

    Leading European Specialist Pharma Company
    Head of Medical Writing and Publications
  • Hard working and there when you need them

    Europe based large biotech
    Regulatory Manager
  • I just wanted to relay our sincere thanks to you and the team for two really excellent days training. It was well organized and structured to cover regulatory expectations, GMP principle and routine work challenges of industry. The presenters and moderator were highly skilled in this area to accommodate any queries raised during the training session and were well able to keep the team engaged even in remote/virtual training session. The design of training slides was impressive and the use of technology to make virtual training was remarkable.

    Lorraine Henry
    Compliance Lead, Qualified Person, Amneal Ireland Limited