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PHARMACEUTICALS
Elevating Drug Research and Drug Discovery for a Healthier Tomorrow
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.
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- Concept Generation
- Detailed Design
- Verification & Validation
- Prototype Development
- Product Documentation
- Design Transfer
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- Remediation
- Corrective action/Preventive action
- QMS Development
- Product design Control
- Superior Quality Assurance Services
- QSR Compliance with 21 CFR 820
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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
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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
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- Remediation
- Corrective action/Preventive action
- QMS Development
- Product design Control
- Superior Quality Assurance Services
- QSR Compliance with 21 CFR 820
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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
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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.