Assessment of POCT Device Potential and Definition of a Go -To- Market Strategy for Selected Countries in South America

News September 27, 2022

AseBio and Alira Health Partner to Foster Market Access for Biotech Startups

Alira Health and AseBio, the Spanish Bioindustry Association, are joining forces to support Spanish biotech companies looking to enter new markets.

Biotech Market Access Startups

Events September 7, 2022

MDIC Annual Patient Forum 2022

We are pleased to share that we will be joining as speakers MDIC Annual Patient Forum 2022 – a key platform for the discussion of how to transform patient engagement throughout the(...)

Clinical Trials MedTech Patient Engagement

News September 6, 2022

Alira Health Expands North American Capabilities with the Acquisition of Artisan Healthcare Consulting

The acquisition of Artisan strengthens and extends Alira Health’s Market Access and Management Consulting advisory practices in North America and globally.

Biotech Market Access Pharma Therapeutics

Events August 31, 2022

BIOMEDevice 2022

We are excited to share that we will be joining BIOMEDevice 2022 as speakers! This event will bring engineers, business leaders, disruptive companies, and innovative thinkers from the(...)

Investor Relations Medical Devices MedTech

Multimedia August 29, 2022

Webinar Replay: Clinical Trial Management in MedTech & Working with CROs

As a MedTech company, understanding clinical trial management is critical, and working with CROs is part of the journey. Join the webinar to learn about this crucial topic.

Clinical Trial Management CRO MedTech

Events August 23, 2022

MedtechVision 2022

Join us at the MedtechWomen MedtechVision Conference, where we will be presenting a state of the Medtech Industry Report with an overview of the innovation and advancement and much more.

Diagnotics MedTech Patient Centricity

Publications August 4, 2022

White Paper: New European Health Technology Assessment Regulation

In this white paper, we provide an overview of this new regulation, including key points of the new European Health Technology Assessment Regulation, its methodology, and its timelines.

MedTech Regulatory