Medico

Close collaboration from idea to operation

At Kilde, we develop automation systems from scratch. We construct each system in close cooperation with the companies for which we are developing solutions. Our experts assist and advise throughout the process, ensuring that together we build a system that addresses your specific needs for efficiency.

Streamlining Medico & Pharma

With tailored automation solutions for Medico & Pharma, processes become more reliable, faster, and less error-prone, which is essential in an industry where quality and safety are paramount.

Benefits of Automation

Increased Precision
Automation reduces human error and ensures accuracy and quality throughout the entire production process.

High Efficiency (OEE)
Efficient processes mean shorter production times and faster time-to-market. We design our automation systems using high-quality components and deliver reliable solutions with high uptime and consistent quality.

Compliance with Regulatory Requirements
With automated solutions, you are better equipped to meet the strict requirements from health authorities (such as the FDA) and adhere to recognized processes and standards like GAMP 5, GMP, ISO 9001, and ISO 14001.

Reduction in Operating Costs
Automating repetitive tasks reduces the need for manual labor and its associated consequences, ultimately minimizing costs over time.

We develop complete solutions that optimize the manufacturing process from component assembly to advanced process solutions.
To ensure high production quality, quality control is carried out on the components and materials used in the final product – as well as on assemblies and processes both during and after production.
For the medical and pharmaceutical industries, quality assurance is an essential process that ensures products and services meet strict standards for efficacy, safety, and reliability. This includes systematic methods for monitoring and evaluating processes, production, and laboratory testing. By implementing quality management systems such as ISO standards and Good Manufacturing Practices (GMP), risks are minimized, and all products are ensured to meet regulatory requirements.
Our solutions collect and analyze production data in real time, providing you with valuable insights to optimize operations and ensure compliance with regulatory requirements.
We ensure that our automation solutions can seamlessly integrate with your existing systems and technologies, enabling rapid and efficient improvements.

Documentation & Validation

At Kilde Automation, we take pride not only in delivering effective and innovative automation solutions but also in providing thorough documentation that supports our clients' needs for quality assurance and regulatory compliance. We understand that documentation is a central part of Medico & Pharma production, as it helps ensure traceability, compliance, and transparency throughout all project phases.

Requirement Specifications and Design
We document all relevant requirements and design descriptions so you get a clear overview of the project goals and the technical solution. This overview is anchored in the RTM (Requirement Traceability Matrix) and refers to documents such as FS (Functional Specification), HDS (Hardware Design Specification), SDS (Software Design Specification), and DQR (Design Qualification Report), which describe the technical details in depth.

Verification and Validation
We ensure that all systems and processes are thoroughly verified and validated according to test protocols that simplify quality assurance and quality control related to Installation Qualification (IQ) and Operational Qualification (OQ). These test protocols can be rigorously verified and validated in accordance with recognized methods and applicable standards such as GAMP 5, ISO 13485, and FDA regulations.

User and Maintenance Manuals
We prepare detailed user guides and maintenance documents that make it easy for your team to operate and maintain the automated solutions.

Traceability and Reporting
Our documentation supports full traceability of all processes and changes through version control, so you always have access to relevant information whenever needed.

GMP (Good Manufacturing Practice)

With many years of experience developing and implementing automated solutions that help our clients optimize production and ensure compliance with applicable regulations.

Kilde manages complex requirements and high standards within Quality Control (QC) and Quality Assurance (QA), which are crucial for ensuring reliable and dependable equipment operation.

Kilde works thoroughly to ensure compliance between equipment and the entire process surrounding validation and documentation.

Turnkey Systems

It is not necessary to have a finished concept or detailed specification to start a collaboration with us. We have extensive experience helping industrial companies identify their automation needs, and we are happy to assist you in designing and developing the project concept based on your requirements.

We deliver turnkey automation systems and take full responsibility throughout the entire project process — from specification to commissioning of the final solution.

We offer the following turnkey systems for the medico industry:

Assembly solutions
Process solutions
Packaging & palletizing

Assembly solutions

We construct special designed assembly lines with standardized and custom-designed elements, ensuring that your solution is optimized for each specific task.

Process solutions

We provide standardized and custom-designed process solutions.

Packing & palletizing

Our innovative packing and palletizing machines automate numerous tasks while simultaneously handling a wide range of product variants.

Scalable automation solutions

Based on your needs, we provide custom-designed automation solutions – from manual workstations to fully automated high-capacity solutions.

Our project model

Kilde is ISO 9001 certified. This means that you are ensured a solid foundation for quality management in the projects you undertake with us. We naturally have high demands for the process and constantly focus on optimizing and improving. We execute all projects with detailed descriptions of requirements for establishment, implementation, and maintenance.

We use the stage-gate model to manage and control the various phases of the project process. All phase-delimited deliveries in our projects are concluded with approval and evaluation before the next phase can commence. This ensures both transparency and optimal decision-making foundations, helping us stay on course for the project.