MRPeasy is a Cloud-based ERP Software for Small to Medium size Manufacturers.
It is a simple yet powerful ERP software with seamless management of production, stock, customers, purchases and the team.
It includes integrated Analytics so you can enjoy clear visibility to your business performance. Follow Customer Orders, Manufacturing Orders, Purchase Orders, Stock Levels and Profiles, Invoices, OEE, Sales, Cash Flow. Understand the individual profitability of manufacturing orders, products, customers, and much more including integration with your accounts systems.
Learnaboutgmp provides knowledge and expertise that empowers life science organisations globally to accelerate growth and remain in an on-going state of compliance.
Our training platform helps companies enter new markets, manage compliance, optimise quality and elevate performance by supporting processes at every stage of a company’s evolution.
Our online training programmes are developed by passionate industry experts aligned with industry regulations and delivered through Learnaboutgmp’s proprietary instructional design and technology process, which employs learning principles and a user-interface design that maximises the understanding and retention of information.
Explic8 Limited has an extended reach in North America partnering successfully over a period of time with JMP Consulting headquartered in Baltimore, MD, USA.
JMP consulting drives performance and compliance in life sciences organisations. We help our clients solve their most complex business challenges relating to regulatory compliance, process efficiency and effectiveness, organisational design, and technology implementation.
Our success stems from the fact that we can engage on a deep level with our clients to truly understand their business problems and work as a collaborative partner to solve them.
We have a successful track record working with both the largest and smallest life sciences companies, and everyone in between.
Explic8 Limited are pleased to have partnered with SoftExpert, a software solution on an enterprise scale which will add real value to our proposition and the performance of our clients.
SoftExpert is a market leader in software and services for enterprise-wide business process improvement and compliance management, providing the most comprehensive application suite to empower organisations to increase business performance at all levels and to maximise industry-mandated compliance and corporate governance programmes.
Founded in 1995 and currently with more than 2,000 customers and 300,000 users worldwide, SoftExpert solutions are used by leading corporations in all kinds of industries, including manufacturing, automotive, life sciences, food and beverage, mining and metals, oil and gas, high-tech and IT, energy and utilities, government and public sector, financial services, transportation and logistics, and healthcare.
SoftExpert, along with its extensive network of international partners, provides hosting, implementation, post-sales support and validation services for all solutions to ensure that customers get the maximum value from their investments.
Explic8 Limited have extensive experience working within the Medical Device industry and fully understand the complexities and requirements to comply with the ever-increasing associated regulations.
Historically, the industry has relied heavily on paper-based archives and a cocktail of different systems and platforms, making validations and post audit events, difficult and costly to administer.
The Meddevo way sets your focus away from documents to content located on local servers or Cloud-based platforms.
With Meddevo, you can manage your technical documentation entirely digitally. Smart Summary Technical Documentation (STED) creates all the necessary documentation for you and monitors its preparedness.
Their digital content-based solution has been specifically developed for the medical device industry and can fully meet the requirements of the EU Medical Device Regulation (EU MDR 2017/745) and the In-Vitro Diagnostic Regulation (EU 2017/746).