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Neurotechnologie

Electronic Quality Management System (eQMS)

Smarter Quality Management Starts Here !

As a partner of a top-tier eQMS provider, we can help you by bringing a powerful, cloud-based solution tailored for healthcare industry.

After an in-depth market evaluation of our team, we selected a partner that offers an affordable, user-friendly system - perfect for small to medium-sized companies that need functionality without the six-figure price tag.

We also strongly believe that in 2025, It is more than time to ditch the paperwork and streamline quality processes with precision and ease. Why?

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Why? To Boost Efficiency: By automating workflows, cut down on manual tasks, and reduce human error—get more done in less time. Reduce Risk: Catch issues early with real-time alerts and consistent process tracking. Stay Compliant: Meet industry standards with confidence—your data stays secure, traceable, and audit-ready Access Anytime, Anywhere: Cloud-based flexibility means your team can work from wherever they are.

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How KS Pharma Services Supports You?

 

We don’t just install the system—we make it work for you. Our team provides:

  • Tailored implementation to fit your needs

  • Hands-on training and expert support

  • Strategic advice to maximize your QA performance

 

We’ve done the research—so you don’t have to.

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Let’s make quality simple, smart, and scalable.

 

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Electronic Common Technical Document (eCTD)

Navigating the regulatory landscape can be complex, but with our trusted eCTD (electronic Common Technical Document) software solution, we simplify the submission process for life sciences companies. Whether you are submitting to the FDA, EMA, or other global health authorities, our solution ensures that your submissions are fully compliant, timely, and efficient.​

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What We Offer: Seamless eCTD Compilation & Publishing: With our robust platform to structure, compile, and publish regulatory submissions in the eCTD format, you can easily adhere to regional requirements and authority-specific guidelines. Global Compliance: Our system supports submissions to key global markets, ensuring consistent quality and compliance across regions. Regulatory Expertise: We work alongside you throughout the submission lifecycle, from planning and dossier preparation to submission and lifecycle management. Lifecycle Management: Maintain and manage variations, renewals, and updates with ease our solution’s advanced lifecycle capabilities, ensuring your regulatory records remain accurate and up to date. Data Security and Confidentiality: We prioritize the confidentiality of your data, operating in secure environments that align with industry best practices and regulatory expectations.

Ready to streamline your regulatory submissions?

Contact us today to learn more about how we can support your product's journey to market.

SOFTWARE

  • Empowering Pharma with Precision Software Solutions
KS Pharma BV

Terlicht 251

9450 Heldergem

+32 53 39 01 01

info@kspharma.eu

Contact us

Contact us

KS Pharma Bv

Terlicht 253

9450 Heldergem

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