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Low Code in Motion: Fill the digital gaps in life sciences manufacturing with our low-code solutions

- Beate Krüger, Director for Business Development Manufacturing & Supply Chain, NNIT.

- Nils Jonescheit, Managing Consultant, Manufacturing & Supply Chain, NNIT. 

Despite the rapid digital transformation of the life sciences industry, numerous processes are still handled with paper or spreadsheets. Custom apps designed on low-code platforms like Tulip, can provide a quick, agile, and compliant solution to fill the digital gaps.

Considering the substantial efforts towards digitalization, there is still a surprising amount of paper involved in the day-to-day manufacturing of drugs and medical devices.

In many pharmaceutical companies and CDMOs, comprehensive digital platforms like MES (Manufacturing Execution Systems), LIMS (Laboratory Information Management Systems), QMS (Quality Management Systems) and ERP (Enterprise Resource Planning) now play a major role in manufacturing, logistics and quality management. Nevertheless, the reliance on paper-based processes remains a stubborn obstacle.

According to Nils Jonescheit, Managing Consultant, Manufacturing & Supply Chain at NNIT, paper is used for numerous tasks that are cumbersome and expensive to solve with the big platforms and systems, e.g. cleaning instructions, logbooks or equipment tracking, to name just a few of the typical painpoints.

In any pharma organization, you can identify hundreds or even thousands of processes that were deemed either too complex or not important enough to include in the MES, LIMS or ERP configuration. It happens much more often than you would think. But when you rely on paper or spreadsheets, harmonization of such processes across the organization as well as digital data collection remains a distant target. You cannot easily share it with the rest of the organization, use it for automation, or access it for analytics and improvement without manually transferring it, says Nils Jonescheit.

Low-code allows teams to quickly digitize their processes

The answer to this dilemma is to replace the paper with low-code applications, which can be designed to address specific needs without the rigidity and complexity of design of larger systems. This can be done via platforms such as Tulip, which provide easy-to-use app designing tools.

Low-code apps built on Tulip can seamlessly integrate into existing IT landscapes, boosting productivity and bridging gaps left by MES and other systems. If you just want to digitize a simple process without the time and complexity needed to adjust a larger system, this is where low-code shines, says Nils Jonescheit.

As the name implies, low-code requires just some limited knowledge of coding and similar IT skills, which means that process specialists, LEAN experts and other people on the floor can be directly involved in building the ideal digital tools they need to perform their work. Tulip also supports an extensive ecosystem of partners like NNIT, that have the experience and industry insights to provide best-practice-based, process-oriented solutions and templates for life sciences customers.

As a typical example, Nils Jonescheit mentions a checklist used for cleaning rooms and preparing manufacturing equipment between batches.

This type of list usually stays on paper, even though ensuring proper cleaning is critical for operational compliance and safety. The main reason: often the cleaning is performed by external partners with frequently changing personnel that don’t have access to the MES platform functions. By converting the checklist to a simple & safe low-code application, the execution result can be fed into the MES and used to verify and document that the equipment has been cleaned before starting a new batch.

 

A digital checklist also enables the use of other types of technology, such as RFID chips to guide equipment management and cleaning processes.

A production floor might contain multiple rooms full of similar-looking stainless steel equipment, each with different cleaning instructions. By identifying the exact location via RFID or a similar sensor technology, the low-code app can match specific room with the correct instructions, significantly reducing the risk of errors and improving process adherence, Nils Jonescheit explains.

Domain knowledge is essential.

While most low-code applications are relatively simple, their potential to provide value and increase efficiency and quality if applied in a consistent and targeted way should not be underestimated, says Beate Krüger, Director for Business Development Manufacturing & Supply Chain at NNIT:

We can see that low-code nowadays has the maturity to connect the entire life science logistics and manufacturing process, across the whole life cycle of a drug or medical device product. This enables pharma companies to focus on their most acute pain points, such as areas where they experience the most quality issues or frequent deviations. You can narrow in and solve very specific problems this way. At the same time, being based on a global instance, it can be very simple and fast to leverage innovation and information across the entire organization and implicitly harmonize the underlying process execution principles.

The Tulip platform is available as private cloud or SaaS solution. However, building low-code apps for life science purposes requires a well-structured process, robust governance, and domain-specific knowledge about the underlying processes and GxP compliance requirements.

Based on an initial understanding of how applications like Tulip fit into your overall system landscape, you can start enabling the application to exchange the relevant data in a simple and standardized way. Making it available for use in the big platform solutions such as MES, LIMS, or ERP or for specific local or global data analytics purposes.

Once the overall benefit potential is understood, a value-based implementation approach will ensure an optimized cost/value ratio all the way through your low-code journey.

And for usage in GxP-governed processes it is essential to have a well-defined, yet streamlined CSV/validation approach in place, so you can ensure that app implementation is safe and compliant without jeopardizing the benefits in speed and simplicity that a low-code platform can provide.

Follow the paper trail

To identify which processes are good candidates for low-code, the easiest answer is: Follow the paper trail. Paper forms, custom spreadsheets or other isolated documents that are required to perform specific tasks are often the most obvious indications of low-code opportunities.

Typically, you have specific, repeating problems on the shop floor and a myriad of paper-based processes, both GxP and non-GxP. These need to be digitized to finally eliminate the paper and the increased levels of manpower required to manage it, says Beate Krüger and continues:

At first, the relevant line-of-business may work with internal technical partners such as IT/OT, MSAT or Engineering to fix the issue via the established platform solutions. But all too often, this is not a suitable solution and the business case simply is not there. This is where platforms such as Tulip come into play. Once made available and validated in the cloud they can very quickly be made available for local use everywhere across the organization.

Another typical area where low-code solutions quickly show their massive benefit potential is the substitution of very targeted, small custom systems, which each address very specific problems in today’s operations but in their sheer number lead to technical jigsaw landscapes, complex and expensive to operate and manage.

By leveraging low-code platforms with the assistance of an experienced and specialized partner like NNIT, life sciences organizations can break down traditional barriers to digital transformation, fostering a culture of efficiency, compliance, and continuous improvement.

What NNIT brings to the table:

  • More than 5 years hands-on experience of applying low-code solutions in the life sciences industry - in GxP as well as non-GxP environments.
  • A resulting library of best-practice process apps.
  • An outstanding process expertise stretching across all process domains from API & Biotech, Cell & Gene, Secondary manufacturing & packaging as well as medical device.
  • A deep understanding of all steps in the life cycle management of a drug product from R&D through the clinical phases to upscale & commercial manufacturing and the digitalization challenges hidden in each of them.
  • A strong track history of successful projects on vertical and horizontal integration of processes including all the typical underlying system platforms (MES, LIMS, ERP, QMS, Logistics & supply chain solutions, Data Analytics platforms, Track & Trace).
  • A fast-track targeted approach to the adoption of low-code solutions from the initial idea through agile implementation, system & app validation to training, go-live and continuous improvement.

 

It is the unique combination of all those elements that makes NNIT the ideal partner for your low-code journey, to ensure success from day one, says Beate Krüger.

Introducing SMARTT by NNIT: Streamlining Manufacturing, Quality as well as Logistics and Supply Chain Processes with Standardized Packages

SMARTT is a suite of standardized packages that aims to revolutionize life sciences operations. Its purpose is to optimize manufacturing processes by addressing common pain points and ensuring compliance.

One of the key features of SMARTT is its managed, comprehensive Library of templates and semi-automated tools. These resources are designed based on industry best practices, which guarantees seamless integration and optimal performance.

SMARTT is built on trusted platforms like Tulip and Microsoft, providing a familiar and robust foundation for digital transformation initiatives. Each component of SMARTT is meticulously crafted to reflect best practices in process understanding and digitalization strategies, empowering organizations to optimize their operations effectively.


By embracing standardized packages and cutting-edge technology, manufacturers can transition from paper-based processes to efficient, digitally-driven workflows. This allows our customers to enhance data accessibility, streamline operations, and mitigate compliance risks. It's time to embrace the future of manufacturing with SMARTT.

Stay tuned for our upcoming Low Code in Motion webinar!

Eager to learn more about our low-code solutions and SMARTT packages? Don't hesitate to contact us directly!