Lomard Medical Appoints Raymond W. Cohen As Chairman

London, UK, 10 July 2013 – Lombard Medical Technologies PLC (AIM:LMT), the specialist medical technology company focussed on innovative vascular products, is pleased to announce the appointment of Raymond Wayne Cohen as Non-executive Chairman, with immediate effect.

Mr. Cohen, a US national and aged 54, has extensive international medical device experience having held several Chairman and CEO positions on the boards of both publicly listed and private life sciences companies in the US and Europe. He is currently Non-executive Chairman of Jenavalve Technology, Inc., a Munich-based developer, manufacturer and marketer of transcatheter aortic valve systems; Nonexecutive Chairman of Syncroness, Inc., a contract engineering firm; a Non-executive Director of Spectrum Pharmaceuticals, Inc. (NASDAQ:SPPI), a developer and marketer of oncology and haematology drugs; a Non-executive Director of BioLife Solutions, Inc. (OTC:BLFS), a manufacturer of biopreservation media for human cells; and a Non-executive Director of LoneStar Heart, Inc., a developer of biomaterials for the treatment of congestive heart failure.

From mid-2010 to late 2012, Mr. Cohen served as Chief Executive Officer of Vessix Vascular, Inc., a developer of a novel percutaneous radiofrequency balloon catheter renal denervation system used to treat uncontrolled hypertension. In November 2012, during his tenure as CEO, the company was acquired by Boston Scientific Corporation (NYSE:BSX) in a structured transaction valued at up to $425 million.

As announced in April, John Rush decided to step down as Non-executive Chairman following the achievement of FDA approval for Aorfix™ in the United States. John Rush remains an active and committed member of the Board as a Non-executive Director.

CEO of Lombard Medical, Simon Hubbert, commented:

“The Board is delighted to appoint a Chairman of Raymond’s calibre and experience. He brings with him extensive knowledge of the medical device sector in the US and international markets, which will serve the Company well as it executes its strategy. We also thank John for his leadership over the last few years and are pleased he will remain with the Company as a valued member of the Board.”

There is no further information to be disclosed in accordance with Schedule Two paragraph (g) of the AIM Rules, save as set out below:

Directorships in the last 5 years:
Jenavalve Technology, Inc*
Syncroness, Inc.*
Spectrum Pharmaceuticals, Inc.*
BioLife Solutions, Inc.*
LoneStar Heart, Inc.*
Cardiogenesis Corp.
Vessix Vascular, Inc.
CardioPolymers, Inc.
Cardiac Science, Inc.
Cardiac Science Corp.

* Current directorship

 For further information:

Lombard Medical Technologies PLC
Tel: 01235 750 800
Simon Hubbert, Chief Executive Officer
Ian Ardill, Chief Financial Officer

Canaccord Genuity Limited
Lucy Tilley / Tim Redfern / Henry Fitzgerald O’Connor / Dr Julian Feneley
Tel: 020 7523 8000

FTI Consulting
Simon Conway / Susan Stuart / Victoria Foster Mitchell
Tel: 020 7831 3113

About Lombard Medical Lombard

Medical Technologies PLC (AIM: LMT), is a medical device company focused on device solutions for the $1.2 billion dollar per annum abdominal aortic aneurysm (AAA) repair market. AAAs are a balloon-like enlargement of the aorta which, if left untreated, may rupture and cause death. Approximately 4.5 million people are living with AAAs in the developed world and each year 600,000 new cases are diagnosed. The market for endovascular stent grafts for this application is expected to grow to $1.6 billion by 2015. The Company’s lead product, Aorfix™, is an endovascular stent graft which has been specifically designed to solve the problems that exist in treating complex tortuous anatomy which is often present in advanced AAA disease. Aorfix™ is currently being commercialised in the EU, and has been approved by the FDA in the US, the first AAA stent graft not of US origin to gain FDA approval. The Company intends to launch AorfixTM with AorflexTM in the US in H2 2013; a coordinated launch event will take place at the VEITH symposium in New York City in November 2013.

The Company is headquartered in Oxfordshire, with operations in Ayrshire and Phoenix, USA. Further background on the Company can be found at www.lombardmedical.com.

We believe the promise of cell and gene therapies starts with the integrity of a single cell

Advancing the future of cell and gene therapy

The human body can heal itself. Cell and gene therapies are designed to augment the patient’s ability to fight disease but only if the living cells behind those therapies remain viable and functional throughout the production processes. At BioLife Solutions, our mission is to protect the integrity of cells and provide trusted tools, services, and expertise that can enable our customers to advance the development and delivery of cell and gene therapies. We believe the future of cell and gene therapies hinges on the integrity of every single cell and we are here to protect that promise.

We understand the technical demands of bioprocessing in this field, and our advanced biopreservation expertise, cell culture optimization products, innovative storage systems, and closed-system manufacturing solutions are designed to enhance process efficiency, maintain cellular viability, and ensure reproducibility at every stage. Whether scaling up from R&D, navigating clinical trials or optimizing cryopreservation protocols for commercial production, we provide the tools and experience to streamline your workflow and safeguard your therapies.

Work with experts who understand your biopreservation challenges

Notch-Right-25px
Notch-Bottom-25px

Collaborative and comprehensive CDMO support

At BioLife Solutions, we partner with leading contract development and manufacturing organizations (CDMOs) to enhance their biopreservation and cell processing capabilities. By providing advanced tools, regulatory support, and process optimization strategies, we empower CDMOs to better serve therapy developers, ensuring quality, consistency, and scalability in cell therapy manufacturing.

Regulatory
readiness

Navigating the complex regulatory landscape of cell and gene therapy requires a proactive approach. BioLife Solutions offers experienced regulatory support to help prepare your biopreservation and cell processing methods to meet global standards. From IND and BLA submissions to compliance with GMP, FDA, and EMA guidelines, our solutions help streamline approval pathways.

Notch-Left-25px
Notch-Bottom-25px

STORE

CellSeal®
CryoCase

Alleviate CGT container challenges like fracture risk, bag burping or high rates of particulates

Notch-Right-25px
Notch-Bottom-25px

Data-driven
decision making

Stay ahead with our comprehensive Evidence Library, a curated collection of scientific publications, white papers, and case studies demonstrating the efficacy of BioLife Solutions’ technologies. Access peer-reviewed research, real-world application data, and expert insights to support your bioprocessing and regulatory strategies.

Insights

May 21, 2025

Designing the Ideal Cryostorage Container for CGT

April 18, 2025

The Cell Summit ’25: A Must-Attend Event for Innovators in Cell & Gene Therapy

March 27, 2025

Optimizing Biopreservation Strategies for Apheresis-Derived Cells in Immunotherapeutic Applications

February 19, 2025

How to prepare early for regulatory submissions from IND to BLA

Preserve, protect and expand cell performance

Mastering
Biopreservation

Ensure Regulatory Submission Readiness

Automate & Close
CGT Processes

Protect & Expand
Cell Performance