Medical Device Usability Engineering. Product and Service Design Innovation Consultancy

Similar documents
Learning from real world use

Authors Heidi Gautschi Alexandre Raynaud Damien Vossion Michael Wade. Digital Patient Engagement. Insights for the Pharmaceutical Industry

Model Based Design Of Medical Devices

EMA experience with the review of digital technology proposals in medicine development programmes

Leveraging Med Device Expertise to Develop Combination Products

peace of mind For from development to commercial supply

WHY ACCOUNTANCY & SOCIAL DESIGN

Industry at a Crossroads: The Rise of Digital in the Outcome-Driven R&D Organization

AI use in European healthcare

INTEGRATING HUMAN FACTORS AND USABILITY TESTING INTO MEDICAL DEVICE RISK MANAGEMENT

Health Informaticians Drive Innovation from Bench to Bedside

Global Harmonization Task Force

"Working Groups for Harmonisation and Alignment in Brain Imaging Methods for Neurodegeneration" Final version

Making a healthier world

How to take advantage of China knowledge base?

Tecan Group. Corporate Update CONFERENCE CALL JANUARY 15, 2019

Welcome to Althea. Welcome to the future of integrated healthcare technology management

NURTURING OFFSHORE WIND MARKETS GOOD PRACTICES FOR INTERNATIONAL STANDARDISATION

Digital Medical Device Innovation: A Prescription for Business and IT Success

CEOCFO Magazine. Pat Patterson, CPT President and Founder. Agilis Consulting Group, LLC

Overview of Health Technology Assessment (HTA) from Asia Pacific Perspective

Remote participation in Question sessions Audio options VoIP

International Presence, Local Expertise. Introductory Presentation

Research Brief. Clinicians and life sciences companies working together: What types of relationships do clinicians find most appealing?

Finn Børlum Kristensen, MD, PhD Director, EUnetHTA Secretariat Danish Health and Medicines Authority (EUnetHTA Coordinator) Copenhagen, Denmark

Innovation and the Changing Practice of Medicine

Leader in Pharmaceutical Films

ORGANISATION FOR THE PROHIBITION OF CHEMICAL WEAPONS

e-care Living Lab - 5 avenue du Grand Sablon La Tronche - FRANCE Tel: +33 (0)

A Focus on Health Data Infrastructure, Capacity and Application of Outcomes Data

A GUIDE TO. Giving a good interview

MEDICAL DEVICE INNOVATION IN GERMANY

EBA Master Class The Benefits of International Collaboration. Steve Morgan Co-Chair, EBA Benchmarking Group

Compliance for Eucomed: The Medical Technology Industry s s Perspective

Patented Medicine Prices Review Board P M P R B GUIDELINES REFORM. 15 th Annual Market Access Summit. Douglas Clark Executive Director PMPRB

Brighten your Expertise

TRACEABILITY WITHIN THE DESIGN PROCESS

Connecting People, Science and Regulation

Roche in Mannheim. The high-tech campus

Integrate, validate, and implement

Leading Design and Contract Manufacturer to the Medical Technology Industry. Med-tech Pharmaceutical Diagnostics.

Mapping Your Success 2013 BSI Healthcare Road Show

What We Heard Report Inspection Modernization: The Case for Change Consultation from June 1 to July 31, 2012

NIHR ROADSHOW FOR MEDTECH SMES

LÜBECK SUMMER ACADEMY HOW DOES AI TARGET CHALLENGES IN HEALTHCARE DIE SPEZIALISTEN FÜR KÜNSTLICHE INTELLIGENZ IM GESUNDHEITSWESEN

Surgical Sutures Market By Product Type [Automated Suturing Devices (Disposable Automated Suturing Devices, And Re-Usable Automated Suturing

Translational scientist competency profile

Telehealth and Digital Technology. Libbe Englander, PhD

Centre for Healthcare Technologies

Keysight Technologies NFA Noise Figure Analyzer. Configuration Guide

Trouble-shooting Radio Links in Unlicensed Frequency Bands TUTORIAL

April By Type of Approach- Transfemoral and Transapical. By Region- North America, Europe, APAC and RoW

Health & Social Care Industrial Innovation

Agilent NFA Noise Figure Analyzer

BIM adoption policies

Smart devices. How to unlock their potential in the real world. Tobias Handschuh, Ernst & Young

Digitalization and TITLE OF. Devices May 2018 PRESENTATION

Imagine your future lab. Designed using Virtual Reality and Computer Simulation

Current Status and Challenges of Bilateral/Multilateral Meetings

Creating the world technology leader in surface solutions under one roof

BIM Policy Development: Different Countries, Common Approaches

Before I talk through the strategy itself, I want to tell you more about why

End-to-End Infrastructure for Usability Evaluation of ehealth Applications and Services

Treasury and Trade Solutions Citi Commercial Cards. A History of Achievement. A Future of Innovation. May 19-21, 2014

Technology and Innovation in the NHS Highlands and Islands Enterprise

Delicate tasks should be entrusted to safe hands: Medical gases from Messer.

Plant Protection Products. Veterinary Medicines. Biocides. Chemicals. Branch out and broaden your horizons

Agilent NFA Noise Figure Analyzer

Encapsulated Transformers 115V + 115V Primary, Low Profile

WORLD LEADERS IN LINEAR MOTION

Presentation. March 2007

15' COMMENCEMENT DAT E 20+ CONTAINERS DELIVERED T H E WAT S O N 18+ PRODUCT TYPES SUPPLIED CASE STUDY 29 DAYS DURATION HOTEL & SERVICED OFFICES

Software as a Medical Device (SaMD)

Nanomaterials: Applications, Implications and Safety Management in the SAICM Context Rob Visser

Medical Technology Association of NZ. Proposed European Union/New Zealand Free Trade Agreement. Submission to Ministry of Foreign Affairs & Trade

National Medical Device Evaluation System: CDRH s Vision, Challenges, and Needs

Power Measurement and Analysis Software

EUROPE March Brussels, Belgium CALL FOR ABSTRACTS. Join Us at the Crossroads of Healthcare. DIAglobal.org/Europe2020 #DIAEurope2020

Michel Tousignant School of Rehabilitation, University of Sherbrooke Sherbrooke, Québec, J1H 5N4, Canada. And

30 A AC/DC Current Probe TCP0030A Datasheet

Advancing Health and Prosperity. A Brief to the Advisory Panel on Healthcare Innovation

VDMA China Management Meeting. Construction Equipment and Building Material Machinery. Tianjin, 21 May VDMA Sebastian Popp

GLOBAL PRO BONO REPORT. Law is essential to creating a just society, but law does not create justice by itself.

Keysight Technologies Essential Capabilities of EMI Receivers. Application Note

Global Perspectives on Clinical Engineering Trends Yadin David, Ed.D., P.E., C.C.E., FAACE, FAIMBE

The Transition to Model-Based Drug Development. Phase 1: Formalizing the Pharmacometric Process

Adapting Data Collection Methods for Different Participants of the User Study: to Improve the Empathic Understanding between Designers and Users

Smart Grid Maturity Model: A Vision for the Future of Smart Grid

Supporting Innovation through Regulation and Science

Medical Education Activities

Building Quality into Medical Device Documentation and Impact of New Device Regulation (Context: Inhaled Drug Devices) v4

FDA Centers of Excellence in Regulatory and Information Sciences

Your Content Your Way

Verification of Technologies Used for the Production of Drinking Water in Canada

_Beileger_Imagebroschuere_engl_ :19 Seite 1 Did you know?

Patient safety and optimal performance:

International Regulatory Harmonization and Medical Technology Innovation. Some personal thoughts

Medical Electronics I S O. Member of Amalthea Group. Switzerland

Digital Health Startups A FirstWord ExpertViews Dossier Report

AUTO INJECTORS & PEN INJECTORS: A USER-CENTRIC DESIGN APPROACH

Transcription:

Medical Device Usability Engineering Product and Service Design Innovation Consultancy

Delivering Meaningful Innovation PDD services Our integration of multiple disciplines means we offer a comprehensive and holistic approach to product and service design that delivers success. PDD services include: PDD is a product and service design innovation consultancy. We work with our clients to innovate new products and services that delight users and help create business growth. Our team of 50 are based in London, Hong Kong and Shanghai. Innovation Training Design Insight Design Strategy People-Centred Research Our core capabilities encompass end-to-end design and innovation services, which we apply in interdisciplinary teams, enabling us to understand and resolve complex human, technology, cultural and commercial challenges. Human Factors & Usability User Experience Industrial Design Prototyping & Verification Engineering Design Technology & Invention Electronics & Software Production Outsourcing Please get in touch to discuss any of the above services in more detail. e. contact@pdd.co.uk t. +44 (0)20 8735 111 2 3 I

Innovation in the medical sector PDD has been developing medical devices for over 35 years, leveraging human-centred design methods to drive innovation from insight through to production. Pharma & Drug Delivery Surgical & Interventional Wound Care Emergency Services Diagnostic & Monitoring Systems E-Health Patient Mobility Our diverse Human Sciences, Design and Technical skills are integrated into a seamless innovation approach that identifies and responds to opportunity and manages risk from early market research through to production transfer. Human Factors & Usability Human factors is not a stage in our process it is a fundamental foundation that runs throughout the course of every project, from desk-based research through to post-market surveillance. Usability Engineering The concept of Usability Engineering (UE) brings together Human Factors, Risk Management and User Experience design to understand and optimise how users interact with medical devices. UE is a regulatory requirement and PDD can fully integrate UE throughout the medical device design and development process or support stand-alone usability testing for your own development projects. 4 5 I

Regulatory Landscape PDD has a comprehensive understanding of IEC62366 and ISO14971 which are both harmonised under the Medical Device Directive. PDD operates in compliance with the FDA and design guidance documents such as HE75. Process In-line with regulatory requirements to develop a UE file for pre-market submissions, we can provide you with a full suite of regulatory documentation to suit the needs of your project. Use specification Usability risk analysis User interface specification User interface plan Formative evaluation Human Factors Usability Engineering IEC 62366 ISO 14971 No Is residual risk acceptable? Summative evaluation Does the benefit outweigh the risk? No Risk Management User HE75 MDD/FDA compliant Yes Yes Experience UE summary report 6 7 I

Human Factors: What we offer Workflow optimisation Ethnographic research Exploratory studies Heuristic reviews Use error risk analysis IFUs Training Formative evaluation Summative evaluation Post-market research On-site facilities There are two usability testing rooms at our London studio. The private rooms can be used for formative or summative evaluations and are equipped with twin ceiling mounted cameras and microphones for recording and remote client viewing. A wide range of use-scenarios can be simulated such as the home, outdoors or hospital environments. Furthermore, our flexible spaces can facilitate focus groups, training sessions, workshops and interviews. Recruitment We only work with experienced recruiters who have an extensive international network of contacts. Our global team has the collective knowledge of recruiting and conducting evaluations in different cultures and languages. We can gain access to a wide range of simulation suites within UK hospitals and have a network of connections with other testing facilities globally. Our London location allows us to take advantage of the scale and diversity of the London catchment area for recruitment. 8 9 I

Our experience Therapy Areas We have evaluated over 1000 participants in clinical areas such as COPD, Hepatitis C, Multiple Sclerosis, Chronic Bronchitis, Emphysema, Asthma, Peripheral Arterial Disease, Psoriasis, Invasive aspergillosis, Haemophilia, Ventilator-Associated Pneumonia, Diabetes, Neonates and Haemophilia. Stakeholders We have worked with a diverse range of stakeholders: Patients, Health Care Professionals (including Physicians/Nurses/Hospital Pharmacists) and Carers. Countries We have conducted formative and summative evaluations in the UK, USA, China, Japan, Germany, Australia, Switzerland, Italy, Spain, Denmark, France, Holland, Brazil, Mexico, Turkey and Belgium. 10 11 I

What our clients say It has always been a great pleasure to work with PDD. The knowledge and experience of PDD on the subject of Human Factors evaluations has been of great value for our projects. I enjoyed the professional and goal oriented way this work has been organized and conducted and I appreciate the focus on your customer s specific needs, the flexibility to accommodate our timelines and the ability of the PDD team to deliver right on target in terms of time and budget. German inhalation therapy device company PDD s work was very useful in helping us to understand what was needed and how best to develop a protocol. Our interaction with PDD was key in identifying and addressing areas of concern we felt there was enormous value in their depth of expertise. PDD worked hard with us to make sure the timetable was met despite delays in finances this was very much appreciated. Swiss Pharma company PDD s excellent processes, timely, unique and innovative approach to our challenges resulted in a very successful and effective outcome for the project. They were extremely professional and always exceed expectations. The cross-functional session PDD held with us was excellent, the prototypes were great, detailed and accurate costings, and the exploration sessions held with pharmacists were extremely informative. Canadian Pharma company High quality work through expertise PDD exactly know what they do. Passionate and enthusiastic PDD love and enjoy what they do. Pleasure to work as a team PDD listen, PDD care, PDD is open minded and value different opinions. US Pharma company 12 13 I

London studio + 44 (0)20 8735 1111 contact@pdd.co.uk www.pdd.co.uk Hong Kong studio + 852 2997 6151 contact@pdd.com.hk www.pdd.com.hk Shanghai studio + 86 21 5265 6990 shanghai@pdd.com.hk www.pdd.com.hk