Main
Coforge: Where AI engineering meets industry expertise.
Learn about our company, our vision and values, and the 45,000+ professionals enabling businesses to harness the power of AI.
Learn more about Coforge
Learn about our company, our vision and values, and the 45,000+ professionals enabling businesses to harness the power of AI.
Learn more about Coforge
Main
Coforge: Where AI engineering meets industry expertise.
Learn about our company, our vision and values, and the 45,000+ professionals enabling businesses to harness the power of AI.
Learn more about Coforge
Learn about our company, our vision and values, and the 45,000+ professionals enabling businesses to harness the power of AI.
Learn more about Coforge
Pharma, medical device and biotech companies face increasing pressure to demonstrate value and justify pricing as they bring new therapies to market. You have to ensure reliable drug development and manufacturing systems, validate safety and effectiveness, and secure compliance for advanced therapies and research.
To compete, you need to redefine how your company works, operate with greater speed and agility, generate robust evidence earlier, prove value in shorter timelines, and rethink how you engage with patients and providers.
Coforge helps life sciences firms do more than transform technology. We enable the culture shift required to dramatically shorten discovery and development timelines.
We deploy AI solutions that improve target identification, optimize biologic design, and enhance predictions around safety and efficacy. We streamline real-time data collection, improve clinical data quality and enable more accurate predictions.
The result? Faster approvals, reduced end-to-end development and post-market timelines, and lower overall costs. Our services include:
The modern pharmaceutical research and development (R&D) landscape faces challenges that impact how new therapies are delivered to patients. To accelerate the development and delivery of life-saving treatments, you need to adopt innovative solutions, new technologies, and a collaborative approach. We work with pharma, biotech and clinical research organizations (CROs) to:
Implement innovative solutions for digital and adaptive trial protocol design, including decentralized or virtual trial management.
Build robust data management systems, advanced analytics and interoperable platforms to extract meaningful insights for improved decision-making.
Leverage cognitive and Gen AI to streamline and expedite R&D and trial operations, including synthetic control arms (SCAs) for trials, patient recruitment, patient engagement, and customized treatment regimens.
Build a regulatory technology landscape to cover regulatory submissions, intelligence, documentation, artwork management, approvals and other workflows.
We ensure that your technology works towards your ultimate goal, delivering new, life-saving treatments to patients as efficiently and cost effectively as possible.
For pharma and life sciences companies, digital experience is a differentiator. To provide a holistic experience for patients and healthcare professionals, you need personalized, customer-centric, emotional touchpoints across every channel.
For your internal teams, digital tools, AI, and data-driven insights can improve productivity, efficiency and consistency, while empowering employees to provide the highest levels of customer experience.
Our digital experience services for pharma and life sciences organizations include:
Build personalized solutions that help patients proactively manage their care through apps, websites, chatbots, and adherence tools.
Customized provider engagement solutions like knowledge portals, self service representative, virtual contact centers, patient 360 and others.
Drive omnichannel marketing initiatives to educate and promote products and services through personalized messaging, content generation, and preferred channels.
Life sciences business processes are complex, cross functional, and always under the lens of regulatory and compliance requirements. You need the speed and agility to bring new therapies to market quickly, ensure quality and compliance, and reduce costs and human errors.
At Coforge, we work closely with pharma, CRO, and CDMO companies to accelerate speed to market by optimizing, globalizing, and seamlessly scaling your business operations. We provide:
In life sciences, errors in critical areas such as computer system validation (CSV) and computer software assurance (CSA) can have serious regulatory and financial consequences.
Coforge helps deliver continuous compliance at scale, protect patients, and drive growth by eliminating error-prone manual processes with automation.
Our services include:
IQ/OQ/PQ authoring and execution
Cloud validation
Agile validation: CI/CD/CT integration with automated regression
SOPs, change control and CAPA
Deviation handling and closure
Mock inspections and vendor qualifications
SDLC documentation and AMS compliance
CSV-CSA transition frameworks and roadmap design
Global validation process harmonization
Consulting for regulatory office setup
MES, SCADA, PLC, DCS and instrumentation
Cleaning and sterilization IT validation
LIMS, CDS and analytical lab software CSV
Packaging and serialization software CSV