Pharmaceutical Technology, Pharmaceutical Technology, July 2022, Volume 46, Issue 7
Pages: 34-36
Point-of-use manufacturing may lead to a big change in the accessibility of medicines globally.
Unexpected occurrences, such as the COVID-19 pandemic, have shone a light on the already existing issue of global accessibility to medicines through traditional means of manufacturing. As technology improves, the industry looks toward how to improve the landscape of medicinal accessibility. Point-of-use manufacturing may have the potential to change the distribution and accessibility of medicines throughout the world, but not without considering some of the challenges that may arise. Pharmaceutical Technology spoke with Peter Walters, director of advanced therapies at CRB, and Maik Jornitz, president and CEO of G-CON, to explore some of the benefits, challenges, and logistics of point-of-use manufacturing.
The flaws of a new manufacturing approach
PharmTech: What are some of the major challenges/obstacles to consider when approaching point-of-use manufacturing of drug products?
Walters (CRB): Point-of-use manufacturing solves the problem of patient adjacency and therapy transport logistics, but typically introduces the problem of a distributed manufacturing model. The design capacity of a point-of-care facility is most often smaller than that of a central production center, and, as a result, the cost effectiveness of having a fully effective support infrastructure must be evaluated. It is typical for functions like QC/EM [quality control/environmental monitoring] testing, warehouse, engineering support, etc. to be stripped from the building and outsourced or supplied from other sites. As a result, it can be difficult to provide and ensure the same degree of quality, consistency, and compliance in a point-of-use facility compared to a centralized manufacturer. While you have possibly solved the issue of patient access and therapy transport, you have introduced logistical issues with maintaining supply chain and support (engineering, maintenance, calibration, etc.) logistics.
Jornitz (G-CON): The past of point-of-use or point-of-care manufacturing has shown certain weaknesses when reviewing cGMP [current good manufacturing practice] compliance and aseptic processing safety. There were many examples which showed flaws, [such as] contamination control strategies, [where] low costs were the focus instead of high quality. These past experiences need to be overcome, [which] can only be done when the new wave of point-of-care systems are of high quality and in compliance with regulatory requirements. For example, process spaces or units still need to have the appropriate cleanroom classification, material, and personnel flows and gowning. Any cleanroom installed base at the point-of-care requires to be of sufficient quality instead of a cheap fix.
Positive impacts to accessibility
PharmTech: How has the COVID-19 pandemic impacted point-of-use manufacturing, in your opinion?
Jornitz (G-CON): Yes, it has; from mobile sample/test units to compounding and filling units to be able to fight the pandemic spread and drug shortages. The pandemic highlighted that we can be more flexible within our processing systems and bring the processing towards the point-of-use. In our experience, it has been very encouraging to see the industry, regulators, and suppliers come together to work on processing solutions, which allow much faster and more flexible capacity build-up.
Walters (CRB): The availability of COVID-19 vaccines in countries not manufacturing a vaccine directly has been challenging and has caused many countries to revisit their philosophies for providing capacity for therapy supply in-country. Some smaller countries have begun government-sponsored facilities for bringing vaccine and critical therapy innovation within their borders to manage against a repeat of the COVID-19 pandemic situation.
PharmTech: How can point-of use-manufacturing facilities improve accessibility to vaccines and other drugs in certain countries?
Walters (CRB): Many pharmaceutical therapies, especially when it comes to sterile injectables, have transport and storage logistics that involve cold chain complications. When trying to manage transport between different countries, factoring in customs and inspections timing, the effective shelf life and efficacy of a therapy can be dramatically impacted by just trying to deliver cross-border. Further, factor in that most countries producing a vaccine are likely going to prioritize their own citizens first. The brutal truth is that smaller countries may find themselves waiting in the queue for therapies to arrive, with reduced usability once they do. In many cases, the ability for these countries to have point-of-use manufacturing centers enables them to begin supplying patients faster and more effectively.
PharmTech: How can modular facilities/point-of-use drug manufacturing impact manufacturing capacity/scalability?
Walters (CRB): The design capacity of a point-of-care facility is typically smaller than that of centralized production facility. The facility is intended to serve a local patient population instead of a global population. Therefore, the scale of production for a point-of-use facility is going to be smaller by design. While smaller production [is] at an individual level, at a global view you can leverage a number of these distributed facilities to make an impact on patient populations.
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Logistics of point-of-use manufacturing
PharmTech: How can a controlled environment be maintained in a modular facility in different climates/smaller production space to ensure consistent drug quality?
Jornitz (G-CON): It all depends on the technology deployed. It is much more difficult to control the environment in a modular facility unit, which was meant for other purposes, for example, transport containers. Cleanrooms are purpose-built, with high quality to be assured that the injectable coming out of such unit is safe for the patient. Mobile units we delivered need to have the right robustness in containment to [ensure] that the processing of the medicinal drug is safe in any outside environment. That starts with temperature, pressure, and humidity controls, which means the air handling units needs to be appropriately scaled, [and] insulation needs [to be] correctly specified and personnel/material flows controlled so outside air cannot penetrate the processing space. This can only be done with high-quality designed and constructed cleanroom systems.
Walters (CRB): There is, at this point, an established history of fully modular manufacturing spaces being able to provide robust cleanroom environments to support GMP processing. The design team would need to account for the site location requirements, and, if the point-of-use facility is intended to be mobile and relocatable, the span of site requirements it may encounter.
PharmTech: What engineering considerations must manufacturers be aware of prior to approaching point-of-care manufacturing in a modular facility setting?
Walters (CRB): Modular builds are fast to erect but come with their own set of design complications. Spaces must adhere to certain dimensional restrictions for shipping purposes, which can implicate how many cleanroom suites and how large they can be. Modular builds can be completely free-standing outside, but this would need to be factored in from the start of design. One prime benefit of the modular approach for point-of-care spaces is that they can be disassembled and relocated to different sites, as befits the point-of-care need.
Jornitz (G-CON): The processing environment requires to be protected in the same way as any other processing space. In [certain] instances, one can see a drift into low quality environments, which requires strict regulatory reviews as there may be weaknesses in containment and stable environmental conditions. That means the design and build of these modular facility settings requires detail and experience to meet the quality and regulatory demands.
Personalized Cell Therapy
Pharmaceutical Technology spoke with Peter Walters, director of advanced therapies at CRB, about point-of-use manufacturing for cell and gene therapy.
PharmTech: How can point-of-use drug manufacturing impact the cell and gene therapy industry?
Walters (CRB): Point-of-use manufacturing could have the potential to improve the personalized cell therapy industry. These therapies suffer from transport logistical issues in moving patient cells from the clinic to the manufacturing facility, and then back again. This transport causes delays to the delivery of the therapy to the patient, introduces cold chain and sheer sensitivity shipping hurdles, and lengthens the time the cells are forced to be stored in a non-ideal state. All of these ultimately contribute to lowering the efficacy of the therapy and the chances the patient will have a successful recovery. Moving the manufacturing activity adjacent to the patient could dramatically reduce these issues, potentially improving the therapy’s effectiveness.
Reflection and looking forward
PharmTech: What technological improvements have occurred that have helped to progress point-of-use manufacturing?
Jornitz (G-CON): The technology improvements happened twofold; single-use process technology enabled closed processes and mobile cleanroom units to deploy such processes to different location or being cloned to a multitude of locations. In addition, the volumes processed, for example in cell therapy, are much smaller, which allowed process intensification and the processing within single-use assemblies within smaller footprint mobile cleanrooms. If the volumes would not have gone down and we would still live in a world of 20,000L volumes, point-of-care processing would not [be able to] happen.
Walters (CRB): The industry push towards Pharma 4.0 and the widespread adoption of automation and digitalization helps drive toward consistent and digitally documented manufacturing. One of the biggest hurdles for a distributed manufacturing model is how to maintain and ensure quality and consistency from site to site. The use of concepts like electronic batch records, online process monitoring, and automated quality testing would go a long way to providing quality assurance and helping negate site to site nuances.
PharmTech: What, in your opinion, do you foresee as being important trends that will impact point-of-use manufacturing in the near future?
Jornitz (G-CON): Three factors will determine the use of point-of-use manufacturing; scalability, controls, and quality. With the possibility of mass-production of mobile progressing units, we can bring costs down and therefore scale such platforms much faster. Controls are needed to keep these processes and units under the robust containment options needed, as well as potentially reduce the human contamination impact. Quality is a must and it starts with the design and construction materials used. Ultimately, the quality benefits will outweigh the cost of bad quality, and that will save patients’ lives.
Walters (CRB): To enable point-of-use manufacturing to go from talking point to reality, facilities are going to need to utilize robust small-scale processing solutions that are automated and digitally integrated. To make the business model viable, manufactured therapies will need to be handled and produced with the same level of quality and care from site to site. Use of automated processes, testing, and digital monitoring will be essential in ensuring quality and consistency across the manufacturing network.
About the author
Alivia Leon is the Assistant Editor for Pharmaceutical Technology.
Article Details
Pharmaceutical Technology Vol. 46, No. 7 July 2022 Pages: 34-36
Citation
When referring to this article, please cite it as A. Leon, “Advancing Accessibility through Point-of-Use Manufacturing,” Pharmaceutical Technology 46 (7) 2022.
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