STIWA Services:
Comprehensive Solutions for Life Sciences
The success of your Life Science product and manufacturing begins with uncompromising quality and extraordinary process reliability. Modern automation systems must combine GMP-compliant processes, complete traceability, and absolute precision in the various cleanroom environment levels. This is exactly where STIWA Automation comes in: We turn complex challenges and strict regulatory barriers into a decisive competitive advantage.
What does this mean for you as a partner?
You receive a GMP-compliant, high precision and extreme quality automation solution that not only increases productivity but also lowers total cost per unit ownership. As an experienced partner, STIWA accompanies you through the entire design, build, validation and qualification process. We proactively deliver all the necessary documents and thus significantly accelerate your market launch.
Precise assembly, careful handling, thorough inspection
Highly automated STIWA machines set standards in the medical technology and the pharmaceutical industry. Continuous production under the strictest cleanroom conditions ensures maximum product compliance to cleanliness, efficacy and safety. Comprehensive quality controls at every stage of production guarantee smooth process flow and flawless product quality.
CLEANROOM EXPERTISE
for your machine project
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RELIABLE PARTNER
for validation
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PROCESS EXPERTISE
for maximum safety
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SCALABILITY
to meet varying needs
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SUSTAINABLE SUPPORT
for long-lasting equipment
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Cleanroom competence
for your machine project
The manufacture of highly technical medical and pharmaceutical products requires a deep understanding of Regulatory Compliance and GMP such as, particle prevention, materials and chemical compatibility and tolerance effects. Cleanroom compliance and competence are implemented in our systems which are designed for deployment in cleanroom classes A-D or ISO standard 5-9.
Sophisticated designs with high-quality materials such as stainless steel, passivated metals, and compliant polymers along with easy access for cleaning and maintenance are standard.
Reliable partner for validation
The responsibility for the timely execution of acceptance tests (FAT/SAT) and delivery of validation documentation supporting qualification steps (DQ, IQ, OQ) are in experienced hands at STIWA. The validation phase is often a critical bottleneck that can jeopardize a timely launch. We transform this process from a potential barrier into a precisely planned milestone.
Your benefits
Accelerated commercial acceptance, secure data integrity, and minimized project risk.
Process competence for maximum safety
True process reliability arises from a deep understanding of the product in each phase. STIWA systems handle the entire process – from precise feeding, assembly and packaging to integrated quality control. Particular attention is paid to the sensitive handling of fragile or valuable products, secured by vision systems and inline measurement technology.
Scalable to meet varying needs
The market requirements in the medical technology and pharmaceutical industry are changing rapidly – from new product variants to fluctuating production volumes. The answer to this is not a rigid system concept, but a well-thought-out modular system that enables fast setup times and simple product changes. Each machine is designed to grow with your needs and integrate seamlessly with higher-level IT systems (MES).
Sustainable support for long-lasting equipment
Successful automation does not end with the start of production. STIWA sees itself as a reliable long-term partner throughout the entire life cycle of your machine and offers global service and support, including the optimization of integrated software solutions. A high degree of standardization ensures short delivery times for spare parts and upgrades.
What does this mean for you?
A high level of machine availability, long-term support and the security of having a competent contact person even after the end of the project.
The process diversity of STIWA automation
The true strength of an automation solution is the mastery of every single process detail. STIWA integrates an exceptional range of technologies to meet even the most complex production requirements. This overview shows a selection of the critical processes that will ensure the success of your product.
PACKAGING & LABELING
SPECIFIC APPLICATIONS
Product package loading, barrier film placement/cutting/sealing, flow wrapping, erecting/filling/closure/sealing/taping of cartons and case packs, labeling in continuous operation of product and cartons/case packs, inserting into trays and materials racks, palletizing
ADVANTAGE FOR SAFETY AND COMPLIANCE
Secure, efficient and fully automated end-of-line processes
