AmpleLogic Electronic Quality Management System (eQMS) is a web-based application helps lifesciences industries to automate and streamline manual paper-based QMS Process and enables quality teams to centrally manage, track and monitor their compliance processes.
AmpleLogic Learning Management (LMS) Software enables you to easily develop and manage learning programs including instructor-led classroom sessions, on-the-job training, and induction programs as well as track, report and deliver them online and offline. AmpleLogic Learning Management System (LMS), you can centrally manage, develop, add, update, and deliver all of your training resources to your learners.
AmpleLogic EDMS is a web-based Electronic Document Management System that automates and seamlessly manages your document management process to ensure compliance by having control of your documents
AmpleLogic Asset Management Software (AMS) Software assists organizations in simplifying calibration processes and complying with regulatory standards governing precautionary maintenance schedules for all instruments. It aids in the planning and generation of prompt notifications for impending equipment re-calibration, the documentation of calibration activities outcomes, and the creation of certificates under regulatory requirements.
AmpleLogic’s Stability Management Software is a comprehensive cGMP software designed to satisfy the demands of biotech, life sciences, pharmaceutical stability testing programs, and stability management. This Stability Management Software helps to simplify and test their organization’s operations and also specify the testing parameters for stability investigations
AmpleLogic Electronic Logbook is a web-based software or platform that records general production requirements and keeps track of Area and Equipment operational usage, Packing, Cleaning, Break Down, Clearance, and Preventive Maintenance, Fogging and Defogging Log, Granulation, Calibration, Equipment Usage, Stability Schedule, Standards Usage, Service Log, Dispensing, Production, Chemical Usage Log, and many other equipment details log. This eLogbook Software is designed to assist users in converting manual paper forms to electronic equivalents. Additionally, the logbook software guarantees that details or log are entered accurately and on time, and that they may be validated, reviewed, and authorized via approval workflows. AmpleLogic Equipment Usage Logbook Software is compliant with FDA regulations governing electronic records and signatures, including 21 CFR Part 11. This solution also complies with other regulatory standards such as EU Annex 11, MHRA, GAMP, Good Manufacturing Practice (GMP), Standard Operating Procedures (SOP’s), and ISO. The software was created having in mind the requirements of major regulatory authorities, and to better serve our clients The AmpleLogic eLogbook Software/Electronic Logbook guarantees that information is disseminated throughout the organization’s essential operational departments including the quality, production, planning, and maintenance departments; and they serve to bring clarity and transparency to the entire organization’s production and QC lab activities.
AmpleLogic Electronic Batch Manufacturing Record (eBMR) Software is designed for pharmaceutical companies to automate manual paper-based batch manufacturing records to ensure compliance.
AmpleLogic Environmental Monitoring System (EMS) Software developed for managing microbiological data of the environmental monitoring programs and also helps to maps your entire sampling workflow.
RIMS (Regulatory Information Management System) allows companies to team up, preserve application information data from various locations and enhance the processes of preparing a submission, as well as simplify the publishing and tracking of all regulatory activities that support a product’s complete life cycle.
Founded in 2010, AmpleLogic has emerged as a pioneer in the Lifesciences Industry, dedicated to being the "One stop shop." Our unique approach integrates IT services and Commercial Off-The-Shelf (COTS) Software seamlessly on the LOW CODE NO CODE (LCNC) PLATFORM, streamlining automation and cutting integration costs. Utilizing cutting-edge 'Low Code No Code (LCNC Development) Platform' technology, our solutions empower organizations to transition from manual to digital operations, fostering efficiency. With a portfolio of 18+ COTS Products compliant with stringent regulatory standards, including USFDA, 21 CFR Part 11, MHRA, EU Annex 11, GMP, GAMP, and ISO, we continue to invest in innovation, launching a minimum of 2 products annually, solidifying our position as a trusted partner in the industry.