MedPharm strengthens management on back of US success
Appointments come as global leader in contract topical and transdermal pharmaceutical development benefits from increased revenues.
MedPharm has appointed Simon Redgrove as Chairman of the Board and Dr Jeremy Drummond as Vice President of Business Development and member of the Executive Leadership Team. The appointments come as MedPharm benefits from increased revenues as a result of integrating services with its fully functioning US laboratory facilities in North Carolina.
Simon Redgrove has built a strong reputation in the financial business community for nurturing the growth of businesses. He will provide overall guidance to the board and brings a depth of knowledge of fostering companies like MedPharm through critical growth stages in their development. Simon was a founder and managing director of Cavanagh Group PLC in 1996 which he took to the AIM market in 2001 and sold to Close Brothers in 2011. Subsequently as Head of Advice at Close Brothers Asset Management he was instrumental in turning around the business. In 2015 Simon cofounded MunnyPot Ltd, a low cost online investment service.
Simon Redgrove stated: “I am delighted to be joining the MedPharm board as Chairman. The company has a solid track record of growth over the last nineteen years. I am looking forward to helping MedPharm grow on the back of the many exciting innovations it is bring to its services to support customers’ development projects.”
“We are very pleased to have secured Simon Redgrave as our Chairman,” said Dr Andy Muddle, MedPharm’s CEO and Co-founder. “We will look to use his different perspective and strong business acumen to ensure MedPharm continues to grow in line with its ambitious strategic plan”.
Dr Jeremy Drummond joins MedPharm having spent over 20 years in roles of increasing responsibility leading the commercial supply of product and services to pharmaceutical companies across the globe. His role is to help clients understand how MedPharm can mitigate risk and shorten their development timelines of their generic or proprietary products. He started his career as a formulation scientist at major multinationals and has a PhD in organic chemistry from the University of Cambridge.
Jeremy Drummond commented: “MedPharm has a fantastic reputation in the pharmaceutical development marketplace and is continuing to bring new ideas to help reduce the cost and reduce the time to market for our customers’ topical and transdermal development programmes. I look forward to helping the team expand these benefits to customers focused on ear, airway and eye indications where MedPharm has demonstrated it has much to offer.”
“Jeremy brings a wealth of experience to the Executive Team”, said Prof Marc Brown, MedPharm’s Chief Scientific Officer and Co-Founder. “His commercial experience and knowledge is strongly complimented by his technical background and we are looking forward to him driving forward MedPharm’s presence in the global pharmaceutical CRO marketplace.”
Related News
-
News Pharmaceutical Supply Chain People Moves
The latest appointments, promotions, and structural changes across the pharmaceutical supply chain.
-
News Merck KGaA to buy US biotech SpringWorks for US$3.9 billion
The German multinational pharmaceutical company Merck KGaA have signed a deal to buy US biotech company SpringWorks Therapeutics at an equity value of US$3.9 billion in a move to add rare cancer therapeutics to their pipelines.
-
News Cassava Sciences halts Alzheimer's drug trial after limited progress
Cassava Sciences have drawn a close to their investigations and development of the drug simufilam, which they intended to be used for the treatment of Alzheimer’s disease.
-
News US FDA adds haemodialysis bloodlines to devices shortage list
On March 14, 2025, the US FDA published an open letter to healthcare providers citing continuing supply disruptions of haemodialysis bloodlines, an essential component of dialysis machines.
-
News Vertex Pharmaceuticals stock jumps as FDA approves non-opioid painkiller
UK-based Vertex Pharmaceuticals saw their stock shares soar as the US FDA signed off on the non-opioid painkiller Journavx, also known as suzetrigine, for patients with moderate to severe acute pain, caused by surgery, accidents, or injuries.
-
News Lessons from CPHI Milan 2024: Sunny Intervals for Pharma Manufacturing?
As the 2024 CPHI conference wrapped up in Milan, we caught up with L.E.K. Consulting – a global strategy consulting firm with deep expertise in pharma manufacturing – to discuss evolving market perspectives and business outlook. -
News US BIOSECURE Act passed by US House of Representatives
The controversial act, which has already impacted several foreign companies operating in the US, was passed by the House of Representatives on September 9, 2024. It is now headed for the US Senate before it can be signed into law by President Joe Biden... -
News Drug prices agreed upon as part of the US Inflation Reduction Act
The Inflation Reduction Act brought into constitution by the Biden administation in 2022, which proposed a drug price negotiation between the government and pharmaceutical companies, has reached it's first agreement.