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To achieve and sustain excellence, a company needs a good quality control system. We provide Internal Quality Audit to helps organizations. Internal Quality audits are typically performed at predefined time intervals as per the audit plan and ensure that the institution has clearly defined internal system monitoring procedures linked to effective action. The audits are unbiased and require cross-functionality of departments.
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Unlock the future of facial recognition technology with our cutting-edge Face Recognition SDK. Designed to empower businesses and developers, our SDK harnesses the power of AI to deliver unparalleled accuracy and speed in identifying faces. Seamlessly integrate our SDK into your applications, websites, or security systems to enhance user experience, improve security measures, an...
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Bet365 clone script is a comprehensive solution empowering entrepreneurs to create sports betting apps and websites reminiscent of Bet365. This bet365 clone script comes equipped with advanced features meticulously designed to emulate the functionalities of the esteemed platform. With Dappsfirm's solution, businesses can seamlessly enter the thriving sports betting market, capitalizing on the established success of Bet365's model.
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Experience seamless quality control with our Integrated Quality Management System. Elevate efficiency and productivity effortlessly. The QMS requirements of the Canadian Medical Devices Regulations are included in the MDSAP. A document outlining the current good manufacturing practices requirements is the FDA 21 CFR Part 820, often known as the Quality System Regulation. A MAVEN integrated quality management system complies not ...
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Create your mulit-player sports betting platform easily with Plurance’s top-notch 1xbet clone script. Our script is the replica of f...
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Make a statement with Jewelry Packaging Mall's shopping bags in stock. Designed with durability and style in mind, our bags are the perfect finishing touch for your customers' purchases.
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We help you to prepare Medical Device Technical File (MDR) as per the regulatory requirement of EU MDR 745/2017 and submit to notified body for review and approval of CE certification. In Bangladesh, the Directorate General of Drug Administration (DGDA) oversees medical devices registration. Operating under the Ministry of Health and Family Welfare, DGDA regulates the import, production, distribution, and sale of medical...
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