Phase II and Phase III Pivotal Trials

Late-stage trials that decide approval. Delivered right.

Med eTech Innovation runs pivotal Phase II and Phase III clinical trials for pharmaceutical, medical device and biotechnology sponsors. Every study is run to ICH E6 Good Clinical Practice (GCP), backed by our dDIB digital tools and preclinical and early-phase depth when your programme needs it. Based in Dundee, delivering internationally.

30+
International partners across five continents
550+
Peer-reviewed publications by our Chief Scientific Officer
2018
Founded in Dundee, Scotland, UK
About Med eTech

Beyond the typical CRO

Pivotal Phase II and Phase III delivery is our core. What sets us apart is the depth behind it: preclinical formulation, PK studies and early-phase work, so sponsors keep one partner from bench to bedside.

Med eTech Innovation provides pharmaceutical, medical device, and biotechnology companies with a responsive and flexible development service. Our management team brings decades of clinical trial experience and global relationships with key opinion leaders to deliver studies on time and within budget.

Our unique business model combines commercial CRO services with a commitment to global health access and equity. For neglected global diseases in low and middle-income countries, we seek cost recovery, not profit. This dual approach gives sponsors access to world-class infrastructure while supporting some of medicine's most underserved populations.

All drug discovery and preclinical work up to Phase I PK/PD is undertaken through our Canadian research partners, leveraging world-class facilities and expertise at the University of British Columbia and the University of Saskatchewan.

Our quality and governance framework aligns with key international standards, including ICH E6 Good Clinical Practice (GCP), ISO 9001 (Quality Management), ISO 13485 (Medical Devices), ISO 27001 (Information Security), ISO 14155 (Clinical Investigations of Medical Devices) and ISO 14971 (Medical Device Risk Management).

Bench to Bedside

Integrated discovery-to-development. Pre-clinical lab, PK studies, Phase I-IV human trials, all under one roof.

Global Health Equity

Ensuring life-saving treatments reach populations in low and middle-income countries who lack access to essential medicines. We run neglected-disease trials at cost recovery, not commercial profit: the same rigorous quality, delivered at humanitarian pricing.

dDIB: Digitally Doing It Better

Proprietary digital tools for clinical data capture, study performance, PI identification, site selection, and patient cohorts.

Scientific Leadership

Led by Director Prof. Christene Leiper and Chief Scientific Officer Dr. Kishor Wasan, co-inventor of Oral Amphotericin B (OAmB) with 550+ publications.

What We Do

Core service areas

From molecule to market. Three integrated capabilities that cover the full spectrum of clinical development.

01

Pharmaceuticals

Pivotal Phase II and Phase III trials are our specialism, with Phase I and Phase IV support available. We also provide pre-clinical laboratory space for drug discovery, formulation, and delivery, PK animal studies, and early-phase human safety and efficacy work including biodistribution studies. Full-service: from study design through to study close-out and post-marketing.

Phase I-IV Drug Discovery PK Studies Data Management Medical Writing Quality & Governance Monitoring
02

Medical Device Trials

Class I through Class III device studies across ophthalmology, endocrinology, respiratory, neurology-stroke, and peripheral interventions. Software-enabled clinical solutions for all your trial requirements, covering the full device classification spectrum.

Class I-III ISO 14155 ISO 20916 Smart Devices Image Advancements Remote Monitoring
03

Digital Solutions (dDIB)

Developed through Onorach Innovation, our parent technology company, dDIB (Digitally Doing It Better) is a proprietary suite of digital tools tackling the five critical areas where CROs under-deliver: clinical data capture, study performance optimisation, PI identification, site selection, and patient cohort identification. AI-powered software reducing cost, saving time, and improving data quality across the trial lifecycle.

Data Capture Performance PI Identification Site Selection Patient Cohorts Blockchain
Therapeutic Expertise

Clinical experience across therapeutic areas

Deep domain knowledge from our leadership team and global network of investigators. Active and completed work across these areas.

Therapeutic Area Capability Coverage
Neglected Global Diseases Parasitic and fungal infections: Leishmaniasis, Onchocerciasis, Chagas, Meningitis, Trachoma
Oncology Solid tumours and haematological malignancies
Cardiovascular PAH, MI, interventional cardiology, hypertension, heart failure, thrombosis, AFib
Nuclear Medicine & Imaging Cardiac imaging, contrast enhancement, diagnostic procedures
Ophthalmology Age-related disorders, novel treatment options, device and pharmaceutical trials
Endocrinology Pre-diabetes, Type I and Type II diabetes, smart device monitoring
Neurology & CNS Stroke, peripheral interventions, cognitive health
Respiratory & IBD GIT studies, respiratory conditions, infectious diseases
Global Reach

Operating from Dundee. Delivering worldwide.

30+
International partners across UK, Canada, Germany, India, Africa
I-IV
Full phase coverage: first-in-human to post-market
I-III
Medical device classes: low to high risk
5
dDIB digital tools tackling CRO underperformance
Leadership

The team behind the science

Combined expertise spanning nuclear medicine, pharmaceutical sciences, drug delivery, and clinical trial management.

Prof. Christene Leiper

Prof. Christene Leiper

Co-Founder & Director

Professor Christene Leiper is Co-Founder and Director of Med eTech Innovation Ltd, Co-Founder of Onorach Innovation, and a Senior Associate of the Royal Society of Medicine. Her career spans more than 40 years across clinical research, nuclear medicine, drug development, stroke care and healthcare innovation.

She was the first woman in Australia to validate the Technegas Easy Breather Accessory (TEBA) for ventilated intensive care patients and conducted pioneering pulmonary imaging research in collaboration with international experts. In Scotland she played a key role in establishing the Scottish Stroke Care Audit, helping drive improvements in stroke services and patient outcomes nationwide.

Professor Leiper has founded and led international contract research organisations supporting Phase I to Phase IV clinical trials, medical devices and digital health innovation. She continues to champion patient-centred clinical research, digital consent technologies, ethical innovation and global collaboration in healthcare.

Senior Associate, Royal Society of Medicine, London
Co-Founder, Med eTech Innovation and Onorach Innovation
Board Member, Oral Amphotericin B (OAmB) Scientific Board
Board Member, International Biodiscovery Forum
Scottish Stroke Care Audit, founding role
Stephen Leiper, Co-Founder, Director and CEO

Stephen Leiper

Co-Founder, Director & CEO

Stephen Leiper is Co-Founder, Director and CEO of Med eTech Innovation and CEO of Onorach Innovation. A fully qualified histologist, he has more than 30 years' experience in diagnostics and molecular research, spanning diagnostic product sales, molecular research tools and clinical research technologies for some of the world's largest molecular research companies.

He co-led the Clinical Trial domain of PharmaLedger with UCB, co-leading the eConsent use case with Boehringer Ingelheim and the Clinical Trial Recruitment use case with Pfizer, and went on to lead eConsent in the PharmaLedger spinout. PharmaLedger was a Horizon 2020 programme funded by the Innovative Medicines Initiative and EFPIA, uniting 12 global pharmaceutical companies to build a trusted blockchain platform for healthcare. Onorach Innovation's eConsent package builds directly on the intellectual property developed in the consortium and is being developed for Med eTech's dDIB digital services.

Stephen is President of the International Biodiscovery Forum, where he speaks on digital health and eConsent.

Co-lead, PharmaLedger Clinical Trial domain (with UCB)
Co-lead, PharmaLedger eConsent (with Boehringer Ingelheim) and Clinical Trial Recruitment (with Pfizer)
President, International Biodiscovery Forum
Co-founded Med eTech Innovation in 2018
Expert in protein electrophoresis (Helena Laboratories)
Dr. Kishor Wasan, Chief Scientific Officer

Dr. Kishor Wasan

Chief Scientific Officer

Dr. Kishor Wasan is a Canadian pharmacologist, pharmacist and academic leader recognised for research in lipid-based drug delivery and global health. He has published more than 550 peer-reviewed articles and abstracts and is co-inventor of a novel oral amphotericin B formulation for systemic fungal and parasitic infections. He serves as Chief Scientific Officer of Med eTech Innovation Ltd.

Current appointments include Distinguished University Scholar and Adjunct Professor, Department of Urologic Sciences, Faculty of Medicine, University of British Columbia, and Co-Founder and Co-Director of the Neglected Global Diseases Initiative at UBC. He previously served as Associate Dean of Research and Graduate Studies at UBC and Dean of the College of Pharmacy and Nutrition at the University of Saskatchewan.

Dr. Wasan is a Fellow of the Canadian Academy of Health Sciences, the American Association of Pharmaceutical Scientists, the Canadian Society for Pharmaceutical Sciences and the Royal Society of Medicine. In 2025 he received both the MD Anderson Cancer Center Distinguished Alumnus Award and the Canadian Society for Pharmaceutical Sciences Lifetime Achievement Award.

Fellow: CAHS, AAPS, CSPS, Royal Society of Medicine
Co-Founder & Co-Director, Neglected Global Diseases Initiative at UBC
MD Anderson Distinguished Alumnus Award 2025
CSPS Lifetime Achievement Award 2025
News & Announcements

Latest from Med eTech

Recognition, milestones, and developments from our team and partners.

25 to 28 October 2026 · New Orleans

Dr. Kishor Wasan to Give Three Presentations at AAPS PharmSci 360

Med eTech Chief Scientific Officer Dr. Kishor Wasan will present three sessions at AAPS PharmSci 360, the annual meeting of the American Association of Pharmaceutical Scientists:

  • From Passion to Practice: Global Health Opportunities for Pharmaceutical Scientists (26 October)
  • Explainable Artificial Intelligence in Pharmaceutical Development and Prescription Medication Safety: Past, Present and Future (27 October)
  • A Novel Oral Amphotericin B Formulation to Treat Visceral Leishmaniasis (28 October)
Events
October 2026

Stephen Leiper Named President of the International Biodiscovery Forum

Med eTech Director and CEO Stephen Leiper has been named President of the International Biodiscovery Forum, a global scientific community connecting researchers, clinicians, innovators and industry partners. Following the 2026 Forum in Varna, Bulgaria, planning is underway for Bengaluru, India in 2027, with Med eTech Chief Scientific Officer Dr. Kishor Wasan among the confirmed keynote speakers. Visit the Forum

Leadership
September 2026

Prof. Christene Leiper Elected to Oral Amphotericin B Scientific Board

We are proud to announce that Med eTech Director Prof. Christene Leiper has been elected to the Scientific Board for Oral Amphotericin B (OAmB) research, recognising her decades of clinical and scientific expertise in nuclear medicine and her contributions to advancing global health research.

Leadership
2025 Awards

Dr. Kishor Wasan: MD Anderson Distinguished Alumnus & CSPS Lifetime Achievement

Med eTech Chief Scientific Officer Dr. Kishor Wasan has been awarded the 2025 UT MD Anderson Cancer Center Distinguished Alumnus Award and the 2025 CSPS Lifetime Achievement Award, recognising his outstanding contributions to pharmaceutical sciences and global health. With over 550 publications and pioneering work on Oral Amphotericin B (OAmB), Dr. Wasan continues to advance the frontiers of neglected disease treatment.

Recognition
August 2026

OAmB (Oral Amphotericin B): Advancing Toward Phase II

Dr. Wasan's novel Oral Amphotericin B (OAmB) formulation continues its development journey. Unlike traditional intravenous Amphotericin B, which carries significant toxicity and requires hospital administration, Oral Amphotericin B demonstrated no significant side-effects and a favourable human Phase 1a/1b safety profile. It is designed to be given remotely and to remain stable in tropical climates. A potential game-changer for treatment access in leishmaniasis and systemic fungal infections across remote and underserved communities.

Research
Get in Touch

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Whether you are planning a clinical trial, exploring a partnership, or want to learn more about our capabilities, we would like to hear from you.

Headquarters

Dundee, Scotland, United Kingdom

Global Presence

Partners across UK, Canada, Germany, India, and Africa

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