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    PHARMACEUTICALS

Elevating Drug Research and Drug Discovery for a Healthier Tomorrow

Digitalization is the key to optimizing R&D and ensuring data-driven decisions across pharmaceuticals. As global medical regulations evolve, many companies struggle to adapt to new standards while integrating new data sources and expensive new technologies. Cyient provides innovative digital solutions, leveraging specialized tools and a strong partner ecosystem to improve clinical efficiency and health outcomes while ensuring compliance. With expertise in clinical data and therapeutic areas like Oncology and Cardiovascular, Cyient offers various solutions in Drug Delivery Devices, Pharmacovigilance, and Real-World Evidence.
End-to-End Solutions

Comprehensive services across the pharmaceutical value chain, including drug discovery, development, and manufacturing.

Innovation and Expertise

Leverage advanced technologies and domain expertise to enhance efficiency and compliance across processes

Regulatory Compliance

Ensure adherence to global regulatory standards, minimizing risks and accelerating market entry.

Digital Transformation

Integrate digital technologies to improve pharmaceutical operations and drive innovation.

Transforming Pharmaceutical with Intelligent Digitalization

Cyient takes complete ownership in the end-to-end of the plant engineering lifecycle, from feasibility analysis to operations and maintenance. We have successfully delivered over 1000 power plant projects globally, leveraging more than 30 years of industry expertise and best practices.

Product to Platform
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  • Concept Generation
  • Detailed Design
  • Verification & Validation
  • Prototype Development
  • Product Documentation
  • Design Transfer
Quality Assurance
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  • Remediation
  • Corrective action/Preventive action
  • QMS Development
  • Product design Control
  • Superior Quality Assurance Services
  • QSR Compliance with 21 CFR 820
Regulatory Affairs
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  • IVDR & MDR Compliance
  • Country specific regulatory filings and submissions
  • Environmental compliance (RoHS, REACH, WEEE)
  • Risk management services per ISO 14971
  • Responding to FDA 483 observations, warning letters, and Notified Body audit findings
  • Post Approval Change Control
Legacy Product Modernization
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  • FHIR
  • Connected Care
  • SaMD
  • IoMT
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  • Concept Generation
  • Detailed Design
  • Verification & Validation
  • Prototype Development
  • Product Documentation
  • Design Transfer
Mask group (29)
  • Remediation
  • Corrective action/Preventive action
  • QMS Development
  • Product design Control
  • Superior Quality Assurance Services
  • QSR Compliance with 21 CFR 820
Mask group (30)
  • IVDR & MDR Compliance
  • Country specific regulatory filings and submissions
  • Environmental compliance (RoHS, REACH, WEEE)
  • Risk management services per ISO 14971
  • Responding to FDA 483 observations, warning letters, and Notified Body audit findings
  • Post Approval Change Control
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  • FHIR
  • Connected Care
  • SaMD
  • IoMT

Elevating Patient Outcomes with
Tech-first Pharma

Pharmacovigilance

  • Big Data Analytics
  • Cloud Solutions
  • AI/ML & RPA
  • Mobile Application

Real World Evidence

  • Patient Engagement
  • Population Health Analytics
  • Data Science

In the Spotlight

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Automation of Clinical Trial Processes and Compliance Tasks

Automated clinical trial processes with UiPath bots, addressing challenges by streamlining processes such as patient data entry, trial validation, and regulatory submissions. Resulting in 300K hours saved annually, reduced errors, and enhanced compliance adherence.

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Automatic Medication (Oral) Monitoring System

Designed and developed the Automatic Medication Monitoring System, providing a complete solution for oral medication management. With an appealing design and easy operation, the system simplifies dispensing, connects patients and caregivers, and stores multiple profiles for comprehensive care.

Make the shift to
INTELLIGENT ENGINEERING

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