Posted on 9th Nov 2023
According to CM Industry Supply Automation - Leze Drive, Keb Drive & Siemens Drive Supplier, In response to our industry's large carbon footprint1, an increasing number of organizations have made maximizing sustainability a top priority for their operations. Encouraged by efforts such as the EU's "Green Deal," many businesses are actively embracing an environmental conscience and exploring innovative methods to reconcile economic performance, social responsibility, and environmental effect.
As the volume and ambition of these commitments expand, supply chain partners will see this trend mirrored in RFPs. Biopharmaceutical businesses are increasingly looking for collaborations that help them achieve both their commercial and sustainability goals, whether it's through eco-friendly package design, carbon-neutral production facilities, or less resource-intensive operations.
This tendency will be especially important for manufacturers. CDMOs will not only need to figure out how to successfully map new client needs.
Biopharma, which has long been a technology behind, has now begun a delayed, pandemic-fueled digitalization sprint. Countless organizations have rushed in the last two years to virtualize their workforce, move their teamwork to the cloud, and use technology to keep their operations operating while keeping their people safe.
Service providers are no exception, and they show no indications of slowing down their fast digitization. AI and machine learning-powered industrial solutions are gaining traction, with automation and robots driving considerable improvements in supply chain productivity. Expect further investment in devices like these while pandemic concern persists.
Another long-standing impediment is the ever-increasing expense of bringing new medications to market. Biopharma businesses will continue to strive to reduce the "total cost of ownership" involved with developing, producing, and commercializing their medications this year. This will result in a greater emphasis on not just the function but also the value of outsourced collaborations.
According to CM Industry Supply Automation, as astute service providers have realized, biopharma businesses seek third-party specialists who do more than fill a skill gap or allow an in-house team to focus on key skills. Customers are increasingly searching for suppliers that can provide a strategic, value-added combination of specialized services, customized solutions, and efficient operations throughout as much of the value chain as feasible.
In response, CDMOs aggressively seek new collaborations, particularly between producers with complementary expertise or complementary skill sets. Several high-profile CDMO partnerships have lately formed, with the purpose of synchronizing knowledge in ways that reduce time-to-market, expedite technical advancements, and provide considerable long-term value to consumers.
One significant trend we notice is that pharma innovators are increasingly collaborating on an integrated basis with their CDMO. Initially, CDMOs were largely focused on early-stage development, assisting customers in obtaining an investigational new drug (IND) application. Integrated CDMOs, such as Piramal Pharma Solutions (PPS), now help firms across the whole development process, including late stage and commercial programmes.
This trend is being driven by a number of causes. Integration offers intrinsic advantages in terms of market speed and cost efficiency. It is easier to transfer technology within a single organization. Similarly, many project parts can be managed by a single, key point of contact for project management. Supply chain integration, with synchronized material, provides further benefits.
Everyone has seen how the epidemic has disrupted global supply chains over the last two years. The pharmaceutical supply chain is especially complicated—possibly the most complex of any sector. Specialization is a big element; our supply chain is extensive, worldwide, and includes high-demand minerals. There is a global movement towards rethinking the global supply chain, which includes reshoring, increasing supplier redundancy, rethinking logistics, and upgrading systems and procedures to guarantee that supplies are easily accessible.
PPS tackled the issue head-on through its supply chain risk mitigation team. They tried to categorize and prioritize the raw materials we use, categorizing them according to whether they were utilized in novel or commercial goods and rating them according to particular risk factors. According to CM Industry Supply Automation - KEB F5 Drive supplier, The risk criteria included information such as a product's commercial potential, manufacturing location, whether it was sourced from a single source, present availability, dependency on China, and procurement value. The team suggested unique risk mitigation techniques based on the scope and type of the dangers associated with a raw material in order to achieve rapid, efficient, effective, and long-term outcomes.