

From inception to final manufacturing and
commercialization.
we can bring your ideas to life or create customise products & designs to fulfil your requirements.


Overview
We at KAIRISH Innotech pride ourselves on offering two key services to support your needs. First, we take the time to fully understand your requirements and then develop a fresh, tailored design and concept to meet your needs from inception to final manufacturing and commercialization. Whether you're developing a completely new product or enhancing an existing one, we can bring your ideas to life or create customise products & designs to fulfil your requirements. Alternatively, if you already have a commercialized product, we can assist you in scaling up production by upgrading your existing machinery or developing more advanced equipment to optimize the manufacturing process. Additionally, if you're looking to scale up the production of an existing device, simply provide us with your tech transfer, quality control protocols, and any other relevant details. We'll ensure that the same high standards are maintained throughout the production process.
We also offer the flexibility to assemble your existing designs and products in our state-ofthe-art facilities. If preferred, you can transfer your machines to our premises, where we will use our ready-to-use assembly areas to enhance your production capabilities. This seamless integration ensures that you benefit from both advanced infrastructure and expert support.

Our Custom or Pre Existing
Technologies For
Commercialization

Creating a New Design Concept to Final Manufacturing and Commercialization


Conceptualization and Design Planning
When a customer requests a completely new product, we start with Conceptualization and Design Planning, which serve as the foundation of the medical device development process. It begins with a comprehensive Needs Assessment, where we collaborate closely with healthcare professionals, stakeholders, and customers to thoroughly understand the specific requirements of the medical device. This includes defining its intended use, target market, and any customer-specific needs, ensuring the product will address real-world challenges effectively. Based on this information, we create a detailed Design Brief, which outlines the product’s functional specifications, performance criteria, and regulatory requirements.
The design brief serves as a roadmap for the entire design phase, guiding the team through the process of turning conceptual ideas into tangible, high-quality medical components that meet both customer expectations and industry standards. When working with a pre-existing design or product, we can either assemble, manufacture, or scale it as needed. This includes assembling machines, injection moulding, or simply receiving components and processing them in designated, classified areas.

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Pre-Production Modelling
Our engineers and designers work collaboratively to develop the initial concept of the medical device. This involves careful consideration of factors such as ergonomics, ease of use, material selection, and compatibility with existing medical systems to ensure that the product meets the practical needs of healthcare providers and patients.
Once the initial concept is defined, CAD Modelling is employed to create detailed 3D representations of the components using advanced Computer-Aided Design (CAD) software. These digital models provide a visual and functional prototype, allowing for preliminary testing of fit, function, and performance before physical production.


Material Evaluation
Material Selection and Testing is a critical step in the development of medical components, as the chosen materials directly impact the safety, performance, and longevity of the product. During Material Analysis, we carefully evaluate and select materials that are biocompatible, durable, and appropriate for the specific medical application—whether for drug delivery, injection, reconstitution, or other uses.
Materials such as medical-grade plastics, rubber, and metals are selected as per their proven performance, ability to withstand stress, and compliance with stringent medical standards.



Prototype Development
Next, prototyping is carried out using rapid prototyping, or the production of small-scale single-cavity moulds and tools. These techniques allow for early-stage testing and validation of the design's feasibility. This iterative process refines functionality, and ensure the product is ready for the next stage of development.



Commercial Production & Scape-Up
Once the product design and final prototype are approved, we have the capability to produce all necessary tooling and machinery—whether semi-automatic or fully automatic—entirely in-house. Our facilities are equipped with dedicated areas for machine installation, offering us great flexibility in customizing setups based on customer needs. We can begin with lowoutput machines for initial production runs and progressively scale up to high-output or mass-production systems as required.
We integrate stringent Quality Control procedures at every stage of the process to identify and rectify any deviations, ensuring that each product meets our high standards. Our cleanroom is certified according to ISO 14644 standards, ensuring a controlled environment that meets the highest levels of cleanliness and safety. This controlled environment minimizes the risk of contamination, especially for devices that will come into direct contact with patients or drug products. We can also operate our machines under Laminar Air Flow (LAF) system.

Regulatory Conformance &
Site Approvals
Regulatory Compliance and Validation are central to our medical device manufacturing process, ensuring that all medical devices meet the highest standards of safety, efficacy, and quality
To comply with regulatory requirements, we prepare and maintain detailed documentation for each product. This includes-Design History Files (DHFs), Device Master Records (DMRs), Risk Management Files.


To comply with regulatory requirements, we prepare and maintain detailed documentation for each product. This includes-Design History Files (DHFs), Device Master Records (DMRs), Risk Management Files.
These documents provide a clear traceability record, demonstrating that each product has undergone rigorous testing and validation to meet regulatory requirements. They also ensure that the devices we produce are safe for their intended use and perform as expected. Certified by ISO 9001:2015 and ISO 13485:2016, which govern quality management and risk management practices throughout the design and manufacturing phases. These certifications confirm our commitment to consistent product quality and operational excellence.
In addition to ISO standards, we are also audited & approved by CDSCO (Central Drugs Standard Control Organisation) for the sterile medical devices that we produce currently. We prepare comprehensive documentation to demonstrate that each product meets the stringent safety, performance, and regulatory requirements. Our Design Validation and Verification processes are critical to ensuring that the product meets its intended use and safety requirements.

These documents provide a clear traceability record, demonstrating that each product has undergone rigorous testing and validation to meet regulatory requirements. They also ensure that the devices we produce are safe for their intended use and perform as expected.
Certified by ISO 9001:2015 and ISO 13485:2016, which govern quality management and risk management practices throughout the design and manufacturing phases. These certifications confirm our commitment to consistent product quality and operational excellence.
