N-SIDE launches Production App to optimise clinical manufacturing process
The software consulting company claims its software solution has already saved one pharma company €10.5 million
Life sciences software consulting company N-SIDE has launched a Production App which it says will further enhance end-to-end clinical trial supply chain management by optimising the pharmaceutical manufacturing process for entire clinical programmes, from drug substance through to drug product and investigational medicinal product.
The company said that with clinical trial supply chains being notoriously difficult to manage due to constantly changing information and large uncertainty in clinical trial demand, multiple teams and siloed data, the new software solution can solve these challenges by considering "all the manufacturing constraints specific to each clinical manufacturing program to deliver the optimal plan and budget."
According to N-SIDE, the app automatically optimizes the usage of production assets and resources to reduce waste, budget and timelines and then facilitates communication of any changes to all stakeholders, worldwide.
"What-if scenario planning allows teams to understand how individual changes might affect the overall situation and proactively model different scenarios to design the optimal plan," N-SIDE said. "With readily available, accurate data, managers can make informed decisions and rapidly adapt to ever-changing clinical plans."
Explaining the app's capability, the company's Life Sciences Director Sébastien Coppe said the app "connects the dots between the strategic vision and the operational decisions for planning your clinical program manufacturing."
N-SIDE said its app has already been tested by a large pharmaceutical company to optimize the clinical trials manufacturing plan for a key biological compound, resulting in an 11% decrease -- or €10.5-million -- in manufacturing costs.
The company added that with ever-changing supply needs and long manufacturing lead times, it is extremely difficult for clinical managers to plan manufacturing to meet these highly variable needs while also minimizing waste, controlling costs and reducing the risk of disrupted drug supply.
"At a program level, this is particularly challenging as multiple trials need to be considered in different global locations, often with a lack of standardization in ways of working and out-of-date or unreliable data on which to base decisions," N-SIDE said.
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.