About Lavida


To become a global category leader in providing state of art pharmaceutical consultancy, and product development services complying with the current international guidelines in the fields of validation, current Good Storage and Distribution Practice (GSDP), current Good Manufacturing Practice (cGMP), current Good Laboratory Practice (cGLP) and for product development / formulation.


Enabling generic pharmaceutical companies to upgrade their knowhow and Tap to new products portfolio thus realizing their potential and growth opportunities in cost effective manner complying with highest Standards and Compliance.

Who We Are

    • An experienced pharmaceutical executives that have the vison to bring unique expertise and add value in Europe in middle east and Africa.
    • We bring real life tested experience on top of qualifications.
    • We have proven track record of excellence.
    • We have tested network and know who to help organizations and bring value to patients.
    • We have uncompromised value for quality and compliance.

LavidaPharma, a registered company in Madeira – Portugal, It is a new concept pharmaceutical focusing on development of generic products from zero base until commercialization it will provide all technical Knowhow as well as market access techniques.

    • Quality management system (QMS) building and compliance consulting services.
    • Product development services from R&D until commercialization.
    • Qualification and validation services.

LavidaPharma work standards will run according to guidlines: