5 research outputs found

    MY Legalis Management System / Muhammad Hanif Nor Azman

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    Dealing with legal firm requires a lot of files to be managed. Although those files are being kept nicely in a drawer, the process of retrieving those file can be quite troublesome and time consuming. The most critical part for a lawyer was deadline issue and the consequences of overlooked deadline may resulting a great loss to both lawyer and client. MY Legalis Management System was proposed to overcome these problems with the features of notification as a reminder to the lawyer. In order to develop the system, a Software Development Life Cycle (SDLC) is chosen and the selected SDLC was traditional methodology, waterfall model. This project covered only first three phases during the development which are requirement gathering and analysis, design and implementation. The system used Java programming language with eclipse as its editor and MYSQL as its database. Web notification was chosen to implement in the system. Due to the time limitation this project cover only conveyancing part and only notify user through web only. Once all the three objectives of the project achieved, the aim of the project is fulfilled and MY Legalis Management System project may help the firm to have a better management on the current business process. This project can be further enhance by expanding the scope into litigation part and email notification

    Utilisation of raw palm oil mill effluent (POME) as a renewable substrate for fermentative H2 production: optimisation using statistical approach

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    ermentative H2 production was studied using raw POME as the substrate with heat-shock pre-treated POME anaerobic sludge acted as the inoculum. The effect of crucial operating variables (initial pH of medium, incubation temperature, and inoculum size) on H2 production was studied using Box−Behnken Design. A second-order polynomial regression model was generated to evaluate H2 production trend under conditions tested. The model analysis revealed the high significance of linear effects of initial pH, incubation temperature, and inoculum size (P < 0.01) towards H2 production. Similar results indicated that the interaction effect between initial pH and inoculum size, and interaction effect between incubation temperature and inoculum size were highly significant (P < 0.01). The regression model suggested that the optimum conditions were set to a pH value, incubation temperature and inoculum size of 6.4, 58.0°C and 8.0% v/v, respectively. In order to validate the optimum conditions determined by the model, heat-shock pre-treated POME anaerobic sludge was incubated with raw POME under optimum conditions. Validation experiment showed that a cumulative H2 volume of 239.0 mL was produced. Microbial community analysis of inoculum showed that mixed consortia between Clostridium sp. and other obligate anaerobic non-spore forming bacteria, mostly belonging to the Firmicutes and Bacteroidetes phyla were identified as the major H2-producers and were hugely responsible towards fermentative H2 production

    Review on Design for Medical Device

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    Medical devices are one of the uprising star in product development due to high demand among users. Developing safe, effective and usable design is indeed a challenging work which faced by designer nowadays. There are comparative methods in designing medical device to achieve desired outcome. Weather designing a “User-friendly”, “Safe to use” or “Eco-friendly” product requires an exclusive method. This review paper might illuminate some light to the designers and researchers who choose to integrate those aspect in their design work in healthcare sector. A review on current method used on user-friendly approach, ensuring safety, regulations on safety of medical device and suggested standards to ensure safety in less complicated way. Thus, there is no solid method or standard yet to establish on safety for medical device

    Review on Design for Medical Device

    No full text
    Medical devices are one of the uprising star in product development due to high demand among users. Developing safe, effective and usable design is indeed a challenging work which faced by designer nowadays. There are comparative methods in designing medical device to achieve desired outcome. Weather designing a “User-friendly”, “Safe to use” or “Eco-friendly” product requires an exclusive method. This review paper might illuminate some light to the designers and researchers who choose to integrate those aspect in their design work in healthcare sector. A review on current method used on user-friendly approach, ensuring safety, regulations on safety of medical device and suggested standards to ensure safety in less complicated way. Thus, there is no solid method or standard yet to establish on safety for medical device
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