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Sudhir Kesavan
January 10, 2024
Sudhir Kesavan

CitiusTech Appoints Sudhir Kesavan as Chief Operating Officer

By MedTech Intelligence Staff

In his new role, Kesavan will assume responsibility for leading CitiusTech’s global delivery organization. This will encompass enhancing practice capability, service delivery maturity, market innovation to drive profitable business growth by collaborating across practices, markets, delivery and functions.

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Northwestern IV Bag recycling program
January 3, 2024
Northwestern IV Bag recycling program

Baxter Advances IV Bag Recycling Pilot for U.S. Hospitals

By MedTech Intelligence Staff

The pilot program launched by Baxter International and Northwestern Medicine in Chicago resulted in the recycling of more than 170,000 IV bags. Baxter is now working to expand the program in the Chicago area to further validate the process and economic viability of the program.

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Caroline Irungu
December 7, 2023
Caroline Irungu

Ask the Expert: Digital Continuity – Strategies for Product Recall Resilience

Class 1 recalls are at a 15-year high. To reduce the number of recalls and nonconformances, medtech manufacturers need quality management and traceability processes that go beyond documenting and tracking changes to effectively connect people, processes and data.  

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Farida Ali
July 6, 2023
Farida Ali
Soapbox

Managing the Post-Pandemic Pricing Squeeze

By Farida Ali

As technology component pricing continues to rise, MedTech manufacturers are applying proven methods and exploring new approaches to maintain profitability and extend product lifecycles.

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Meggan Duffy and Julianne Hartzell
February 28, 2023
Meggan Duffy and Julianne Hartzell

Protecting Innovation in FemTech

By Julianne Hartzell, Meggan Duffy

How innovators in the femtech space can protect their inventions and defend market share.

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Thomas Skogen
January 3, 2023
Thomas Skogen
Soapbox

Risk Management Is More Than a Spreadsheet

By Thomas Skogen

Mitigating risk of failure is one of the most important disciplines to perform for medical device manufacturers, and for the last couple of years, it has become an increasingly difficult discipline to master.

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Mohamed Benkirane
September 21, 2022
Mohamed Benkirane
MEDdesign

Raising the Bar on Quality for MedTech Production

By Mohamed Benkirane

Inspecting for quality after a process is completed is reactive and outdated. Instead, the future lies in predicting quality and quality issues. For medical device manufacturers, the advantages in predictive quality are so great they simply cannot be ignored.

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Big Data
July 6, 2022
Big Data

Addressing Data Challenges in MedTech

Data analytics can provide a more streamlined view of your customers and simplify the complex challenges faced by medical device commercial operations teams.

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Inga Hansen, Managing Editor
June 6, 2022
Inga Hansen, Managing Editor

Innovative Publishing Names Inga Hansen Managing Editor of MedTech Intelligence

Innovative Publishing names new face for MedTech Intelligence

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Tara Lysechko, Starfish Medical
December 21, 2020
Tara Lysechko, Starfish Medical

Does Your Class II Device Qualify for a 510(k) Premarket Notification Exemption?

The exemption reduces the regulatory burden on the medical device industry—including the time and costs involved in preparing, submitting and responding to requests for additional information.

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Columns

November 9, 2025

What is a Service+Tech Model?

By Lakshmeenarayana Goundalkar (LGG)
AI Compliance in Medical Devices

The Service+Tech model embeds AI into the workflow of regulatory experts rather than treating technology as a standalone tool; an approach allowing organizations to adopt AI immediately, with no risk and no R&D investment, while keeping full confidence in the accuracy and regulatory readiness of submissions.

October 28, 2025

Beyond Batteries: The Urgent Case for RF-Powered Medical Devices in Modern Healthcare

By Dr. Charles Greene
Battery-Powered Medtech

Hospitals are adding more connected devices than ever before—from patient wearables to asset tracking systems. Yet this digital transformation is being bottlenecked by an antiquated power infrastructure dependent on single-use batteries that create waste, demand constant maintenance, and compromise device reliability.

October 15, 2025

Disruptive Innovation in MedTech: Evolving Characteristics and Modern Realities

By Partha Anbil
Disruptive Innovation in MedTech

Converting promising technologies into durable outcomes, experience, and cost at scale with evolving technologies and disruptive innovation.

October 13, 2025

Product Development Outsourcing Needs Speed, Safety & Certainty

By MTI Marketing Staff
medtech development

Seek partners who can see your vision — the full picture, anticipate challenges, and help you navigate complexity with confidence.

September 26, 2025

Managing MedTech Cost Pressures With Data-Driven Lifecycle Intelligence

By MedTech Intelligence Staff, Rene Zoelfl
Product Lifecycle Management

To navigate increasingly complex global regulations and rising market expectations, organizations are embracing the Intelligent MedTech Lifecycle: a unified, data-driven approach that breaks down silos and drives agility across the entire product journey.

August 28, 2025

Significance of Harmonized standards

By Rajani Kumar Sindavalam
medtech design standards

The importance of harmonized standards and how they will help the medical device manufacturers in developing devices that are safer and effective.

August 13, 2025

Redesigning Healthcare for a Sustainable Tomorrow

By Andrew Chang
Sustainable medical devices

The future of healthcare depends on cross-sector collaboration among regulatory, commercial, R&D, and business development teams. This integrated approach is crucial to avoiding siloed decisions that could hinder long-term progress. Sustainability must be embedded throughout the product life cycle—from design and manufacturing to distribution and use—ensuring products not only restore sight but also address pressing environmental and logistical challenges.

August 13, 2025

The Hidden Cost of Siloed Hardware and Firmware in MedTech

By Ed Becze, Ron Cassar
collaboration

When hardware and firmware are developed by separate vendors, diagnosing issues like symptoms of non-performance becomes slower and more complex. Unified engineering teams are essential to MedTech success.

TOPICS

  • Digital Health
  • MedTech Economics
  • Manufacturing Execution
  • Product Design & Development
  • Quality/Regulatory

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