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Future of Healthcare

The global healthcare market is growing at a CAGR of 8.9% to reach USD 11.9 trillion in 2022 from USD 8.45 trillion in 2018.

As the healthcare industry evolves, medical devices, pharmaceutical, and digital health companies shift their focus to care affordability, accessibility, quality, and efficiency. Businesses are utilizing the latest technologies to lower the cost of operations and improve process efficiencies. Secure connectivity, automation, and data analytics will potentially increase patient value and decrease disease burden on society.

The Road Ahead

Latest Techology, Partnership and Media updates

Insights & Experiences

A web-based remote doctor-patient consultation application
Case Studies

A web-based remote doctor-patient consultation application

Re-engineering of high power laser-based therapeutic device
Case Studies

Re-engineering of high power laser-based therapeutic device

30% increase in regulatory function productivity of a European biotechnology company
Case Studies

30% increase in regulatory function productivity of a European biotechnology company

EU MDR transition for packaging & labeling function of a leading cardiovascular product manufacturer
Case Studies

EU MDR transition for packaging & labeling function of a leading cardiovascular product manufacturer

Reduction in turnaround time by 20 – 25% for CER creation
Case Studies

Reduction in turnaround time by 20 – 25% for CER creation

Software feature development for anesthesia care product
Case Studies

Software feature development for anesthesia care product

On-prem to Azure cloud migration for hospital workforce and resource management system
Case Studies

On-prem to Azure cloud migration for hospital workforce and resource management system

Custom Android platform-based secondary display for a medical device
Case Studies

Custom Android platform-based secondary display for a medical device

Verification & validation of infusion pumps leading to 20% reduction in time to market
Case Studies

Verification & validation of infusion pumps leading to 20% reduction in time to market

Automation testing of electrosurgical system application resulting in 30% reduction in cost of quality
Case Studies

Automation testing of electrosurgical system application resulting in 30% reduction in cost of quality

Evaluation and integration of X-ray generator with Extracorporeal Shockwave Lithotripsy device
Case Studies

Evaluation and integration of X-ray generator with Extracorporeal Shockwave Lithotripsy device

Re-engineering of blood coagulation analyzer resulting in 35% BOM cost reduction
Case Studies

Re-engineering of blood coagulation analyzer resulting in 35% BOM cost reduction

Value Engineering Feasibility for Breast Pump
Case Studies

Value Engineering Feasibility for Breast Pump

Design & Development of Automated Infusion System
Case Studies

Design & Development of Automated Infusion System

ROHS2 compliance for drug delivery device
Case Studies

ROHS2 compliance for drug delivery device

Next-gen Wireless Stethoscope

Next-gen Wireless Stethoscope

Bluetooth Accessory for Hearing Impaired
Case Studies

Bluetooth Accessory for Hearing Impaired

EU MDR gap assessment & remediation of 330+ surgical product families in a span of 11 months
Case Studies

EU MDR gap assessment & remediation of 330+ surgical product families in a span of 11 months

Updating the CERs as per EU MDR guidelines (Class II and III)
Case Studies

Updating the CERs as per EU MDR guidelines (Class II and III)

Clearing complaints backlog of 15000+ recall products within a span of 7 months
Case Studies

Clearing complaints backlog of 15000+ recall products within a span of 7 months

Reduced turnaround time by 25% by ensuring quality deliverables for PMS documentation as per EU MDR
Case Studies

Reduced turnaround time by 25% by ensuring quality deliverables for PMS documentation as per EU MDR

Centralized label management software leading to 30 – 35% increase in efficiency
Case Studies

Centralized label management software leading to 30 – 35% increase in efficiency

Remediating sterile and non-sterile packaging for medical devices
Case Studies

Remediating sterile and non-sterile packaging for medical devices

Reduced up to 70% manual efforts and 50% operational cost through automated pharmacovigilance workflow
Case Studies

Reduced up to 70% manual efforts and 50% operational cost through automated pharmacovigilance workflow

50% cost reduction with blister packaging design
Case Studies

50% cost reduction with blister packaging design

Clinical labeling documents as per regional guidelines
Case Studies

Clinical labeling documents as per regional guidelines

Published 800+ submissions and 70+ minor and major variation submission for a leading global pharma company
Case Studies

Published 800+ submissions and 70+ minor and major variation submission for a leading global pharma company

An agile, sustainable, and scalable lifecycle management operations for the regulatory function of a US-based pharma
Case Studies

An agile, sustainable, and scalable lifecycle management operations for the regulatory function of a US-based pharma

40% improvement in compliance cost for a Japan-based pharmaceutical company
Case Studies

40% improvement in compliance cost for a Japan-based pharmaceutical company

Smart Wearable Device Concept for Autism and Alzheimer’s
Case Studies

Smart Wearable Device Concept for Autism and Alzheimer’s

Drug Delivery Pen
Case Studies

Drug Delivery Pen

Connected medical devices: A case for Remote Patient Monitoring
Whitepaper

Connected medical devices: A case for Remote Patient Monitoring

IoT-based solutions for healthcare applications
Whitepaper

IoT-based solutions for healthcare applications

Medical Device for Emerging Markets: Potential Indian Market
Whitepaper

Medical Device for Emerging Markets: Potential Indian Market

MDR/IVDR Program Management – Agile Way
Technical Whitepapers

MDR/IVDR Program Management – Agile Way

Decoding the New European Union In-Vitro Diagnostics (IVD) Medical Device Regulation 2017/746
Technical Whitepapers

Decoding the New European Union In-Vitro Diagnostics (IVD) Medical Device Regulation 2017/746

Unfolding the EU MDR through the Lens of a Remediation Partner
Whitepaper

Unfolding the EU MDR through the Lens of a Remediation Partner

Global Regulatory Requirements and Manufacturers Responsibilities for Medical Device Vigilance Reporting
Whitepaper

Global Regulatory Requirements and Manufacturers Responsibilities for Medical Device Vigilance Reporting

Adverse Event Reporting: Power of AI Enabled Cognitive Case Processing and Process Automation
Whitepaper

Adverse Event Reporting: Power of AI Enabled Cognitive Case Processing and Process Automation

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