Feature Prioritization Or Conjoint Analysis

Prioritize Features That Drive True Adoption

Feature prioritization and conjoint analysis

We help you answer questions like:

Which features create the highest adoption impact?

What trade-offs are clinicians willing to make?

Which feature upgrades justify higher pricing?

How do preferences differ across segments (specialty, region, facility type)?

How Cetas Healthcare Performs Feature Prioritization & Conjoint Analysis

01

Attribute Definition

We work with your clinical, R&D, and marketing teams to identify meaningful attributes such as:

  • Device performance parameters
  • Workflow efficiency
  • Safety enhancements
  • Connectivity / digital features
  • Costs & pricing models
02

Attribute Level Development

We define realistic variations of each feature, ensuring validity and regulatory feasibility (e.g., depth of energy delivery, dose ranges, battery duration, sensitivity thresholds).

03

Choice-Based Tasks

We design robust experiments where clinicians evaluate product configurations and make preference-based choices. This reveals:

  • Trade-off behaviour
  • Utility scores for each feature
  • Thresholds for acceptable compromises
04

Segmentation Analysis

We compare results across:

  • Clinical specialties
  • Facility types
  • Experience levels
  • Geographic regions
05

Pricing & Value Modeling

We quantify the perceived value of each feature to support:

  • Price optimization
  • Tiered product strategies
  • Feature bundling

Case Studies

Customer VOC on a new value-PACS product and its pricing
New Value-PACS

Customer VOC on a new value-PACS product and its pricing

We identified the ideal value-PACS package, validated must-have features, and derived the most acceptable price points for emerging markets. The insights enabled the client to finalize a winning product configuration and size the opportunity across... Read More

Delivered robust market size and growth projections for GI-ET procedures and devices

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Cetas Healthcare is the world’s leading boutique MedTech market research firm. We blend agency-grade research with strategic intelligence frameworks to track pipelines, regulatory shifts, clinical trials, and GTM strategies. As pioneers of ISO 14155-compliant PMCF surveys, we’ve managed 25,000+ patient case forms for Class II & III devices, helping clients secure CE certifications and stay ahead of EU MDR requirements.