Cloudtheapp Inc. “A provider of Configurable Quality Management & Regulatory Compliance Software Solutions” is delighted to publicize the release of our renovated Regulatory Dossiers and Submissions Module, allowing businesses to digitalize regulatory processes around establishing dossiers of documents to comply with regulations, and to track submissions to relevant agencies and regulatory bodies.
With widespread availability in Cloudtheapp Store, our valued clients can download and try the module with a click of a button. The module seamlessly blends with all other modules in the RIM and QMS solutions.
“Organizations in Pharma, Med-Device, and many other industries can benefit from the newly unleashed module. Whether your regulatory squad is putting together a pharma dossier of Common Technical Documents (eCTD) for a New Drug Application (NDA), or a med-device dossier for a 510(k) Premarket Notification, the new module would streamline the whole process for you”, said Wael Zebdeh, CTO of Cloudtheapp. “With the release of our renovated module, organizations can be in a desirable position of power to govern regulatory dossiers holistically and in a compliant manner, and to handle and track initial submissions and amendments to agencies like FDA, EDQM, MHLW, and many others across different countries.”
With Cloudtheapp, Regulatory processes to introduce new drugs and med-devices to markets will be simplified, systematized, and digitalized. We help our customers unclose the entrance of digitally possible with the takeoff of the renovated module!
Start with defining the template for your regulatory dossier specifying the modules and sections as instructed by the regulatory bodies. Create live dossiers out of your templates linking to relevant documents, and end up with a journey that streamlines and automates the submission process to regulatory agencies.
Regulatory dossiers and submission activities that are carried out would result in priceless data, and with the power of Cloudtheapp’s integrated real-time analytics, organizations have the chance to drill down on this data visually to identify trends and patterns and make important conclusions that enhance the regulatory processes further. Furthermore, with the power of the Cloudtheapp Platform, businesses can tailor the design of the new module and other integrated solutions to fit their exact needs without having to write code or deal with unknown technologies.
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Cloudtheapp is a No-Code Cloud Platform built for the compliance world. Our vision is to provide you with the most configurable easy-to-use Quality Management and Regulatory Compliance SaaS software on the market. Start with our ready-made applications, use them as is, or configure every aspect of their design, but don’t stop there; using our Validated Compliance” No-Code” platform we want you to automate every other internal process you have, build an application for it, without writing a single line of code or script, and without any additional installs or infrastructure, then see the magic of how ALL applications would integrate to complete your compliance story.
Cloudtheapp has been founded by experienced professionals who have a proven track record in building successful global software. Three decades of industry experience helped us create the most sophisticated compliance & digital transformation tool to bring solutions that address real challenges for the compliance industry.
Our solutions allow you to reach out to suppliers, auditors, consumers, or any other external party, assign them records, get their feedback, and collaborate without the hassle of separate disintegrated solutions and tedious back and forth emails.
Cloudtheapp is light to operate and administer so that your staff can focus on building your quality products.