Paperless QMS Platform
Transform the way you manage quality through digital innovation.
Batch Record Review
Maintain meticulous records that guarantee compliance with GMP standards.
Drug Product Release
Simplify the release process while ensuring safety and efficacy for your end-users
Supplier Qualifications
Ensure a consistent supply chain through rigorous assessment and qualification.
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Why Choose Us?
Our dedicated team of experts brings years of experience in quality assurance, regulatory compliance, and technology integration. We understand the unique challenges faced by biotech and pharmaceutical companies and are committed to providing tailored solutions that fit your specific needs. By choosing Kamosys, you opt for a partner who shares your vision of excellence and is willing to go the extra mile to help you succeed.
Are you ready to ensure that your products meet the highest standards of quality?
Contact Us Today to Learn More About Our GMP Services!
Start your journey towards quality excellence with Kamosys and stay ahead in the competitive landscape of biotech and pharmaceuticals. Together, we can make quality your strongest asset.
Philipp Hahn, CEO Kamosys
Supplier Qualification
In today's complex supply chain environment, having reliable partners is essential. Our rigorous supplier qualification process ensures that all materials and components meet the highest quality and regulatory standards. We evaluate our suppliers on various criteria, including quality assurance processes, compliance with Good Manufacturing Practices (GMP), and their track record in service delivery. By trusting us to manage your supplier qualifications, you can focus on your core competencies and ensure the integrity of your product from the start.
We initiate the process by rigorously qualifying suppliers to ensure that all raw materials and components meet the highest industry standards. Our multi-faceted qualification process includes audits, performance assessments, and compliance checks that help you build a reliable supply chain.
Batch Record Review
Quality is at the heart of every successful product. Our batch record review process meticulously examines all documentation related to each production lot, ensuring compliance with industry standards and regulatory requirements. We take pride in our thorough review, checking for accuracy, completeness, and adherence to established protocols. This not only guarantees that your batches are compliant with GMP but also enhances product reliability and safety.
Once production starts, our expert team conducts detailed batch record reviews to verify that every batch produced complies with regulatory requirements. This meticulous attention to detail mitigates risks associated with quality failures and ensures product integrity.
Drug Product Release
The drug product release process is critical for ensuring that your products are safe, effective, and compliant with regulatory standards. Our dedicated team streamlines this process, enabling timely product release while maintaining rigorous oversight. We focus on ensuring that every product batch is thoroughly evaluated before it reaches the market, minimizing the risk of non-compliance and protecting your brand and reputation.
Our streamlined drug product release processes ensure that you get timely access to your products without compromising safety. Our team works closely with you to conduct all necessary evaluations prior to market release, safeguarding your brand and maintaining customer trust.
Paperless Quality Management Platform
In an age of digital transformation, our state-of-the-art paperless quality management platform revolutionizes the way quality control is conducted. This system ensures integer data management and enhances efficiency by digitizing documentation and automating workflows, ensuring that all quality-related processes are traceable, transparent, and compliant.
With our paperless platform, you enjoy real-time visibility into quality metrics, audit trails, and compliance statuses, which ultimately leads to improved decision-making and reduced time to market.
By moving away from paper trails, you can significantly enhance efficiency and reduce the risk of errors
Chat with our Specialists
You need more information about our services and wish to communicate directly with our specialists?
Book Free Webinar
Check out for one of our free Webinars on supplier qualification and other GMP topics
Ask a question
Contact us via our chat bot or send us your questions via this communication form.