PLM for Pharma

Cut Time, Minimize Risk, Improve Margins

Effectively manage Lab-to-Launch processes for drug commercialization using PLM for Pharma

With drug development and production facing increasing compliance pressure, complexity of disparate R&D facilities and growing competition, clients leverage Wipro’s PLM for Pharma to reduce risk, accelerate market launch and increase product success. Our PLM services include:

Drug Development Portfolio Management: Wipro helps its clients effectively manage their drug development portfolios and provides processes and solutions to improve visibility and tracking of multiple product programs, eventually improving time to market.
Specification Management and Electronic Regulatory Submission: Wipro has built solutions on PLM platforms to develop structured archives which store historical data, facilitate re-use of Common Technical Documents (CTD) and support electronic regulatory submission requirements for FDA & EMA.
Integrated Quality Management: Wipro implements PLM based quality management solutions to track and manage product quality from discovery through commercialization with adherence to FDA and EMA standards (21CFR Part 820). Wipro also delivers validated PLM solutions for DQ, IQ, OQ & PQ requirements.
Global Packaging Management: Wipro provides services on managing digital assets such as artwork and labels, logos and packaging components such as blisters, leaflet, folding box for SKUs, product dossiers and dispensing equipment, enabling clients to achieve an integrated product development and commercialization process.

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