LALAL.AI
Any audio or video can be extracted to extract vocal, accompaniment, and other instruments. High-quality stem cutting based on the #1 AI-powered technology in the world. Next-generation vocal remover and music source separator service for fast, simple, and precise stem removal. You can remove vocal, instrumental, drums and bass tracks, as well as acoustic guitar, electric guitar, and synthesizer tracks, without any quality loss. You can start the service free of charge. Upgrade to get more files processed and faster results. Only for personal use. Move to the next level. You can process thousands of minutes of audio and/or video. This software is suitable for both personal and business use. Each LALAL.AI package has a limit on the amount of audio/video that can be split. The package minute limit is deducted from each file that has been fully split. You can split as many files you like, provided their total length does not exceed the minute limit.
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LTX Studio
From ideation to the final edits of your video, you can control every aspect using AI on a single platform. We are pioneering the integration between AI and video production. This allows the transformation of an idea into a cohesive AI-generated video. LTX Studio allows individuals to express their visions and amplifies their creativity by using new storytelling methods. Transform a simple script or idea into a detailed production. Create characters while maintaining their identity and style. With just a few clicks, you can create the final cut of a project using SFX, voiceovers, music and music. Use advanced 3D generative technologies to create new angles and give you full control over each scene. With advanced language models, you can describe the exact look and feeling of your video. It will then be rendered across all frames. Start and finish your project using a multi-modal platform, which eliminates the friction between pre- and postproduction.
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IQVIA
Numerous organizations globally rely on IQVIA to accelerate the drug development process, guarantee the safety and quality of products, enhance commercial efficacy, deliver appropriate treatments to patients, and ultimately promote improved health outcomes by facilitating access to and delivery of healthcare. Transform your approach to clinical development by seamlessly integrating data, technology, and analytics to streamline your trials. The outcome? Quicker decision-making and minimized risks, enabling you to provide transformative therapies at a faster pace. With its expertise rooted in data, sophisticated analytics, and deep industry knowledge, IQVIA offers tailored capabilities to clients throughout the healthcare landscape. Stay informed by exploring the latest insights and updates from IQVIA's data scientists, healthcare professionals, researchers, and other industry experts on crucial topics that resonate with your interests. From emerging industry developments to practical applications of our capabilities, a wealth of information awaits you here. Engaging with this content also empowers you to stay ahead in a rapidly evolving healthcare environment.
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Astracore Clinical Trials
Our clinical trials management platform is designed to accommodate nearly any type of controlled clinical trial, including those that are randomized, and offers a variety of randomization algorithms. This software can be effortlessly set up for both paper Clinical Report Forms (CRFs) and electronic CRFs (eCRFs). It is capable of capturing data in numerous formats and methods, applying specific guidelines you establish to ensure data integrity and quality control. The system facilitates direct Electronic Data Capture (EDC) through eCRFs or allows for the printing of paper CRFs that can later be input into the platform. Additionally, users can upload various media such as images, audio, video, and documents like consent forms, with the only limitation being the available storage capacity. The system supports Double Data Entry and features comprehensive exception reporting. Moreover, it includes a functionality to lock records after they have been verified, ensuring that no further alterations can be made. This robust capability enhances the overall integrity of the data collected throughout the trial process.
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