Explic8 Limited are pleased to have partnered with the companies below.
Enterprise scale software and cloud platforms which add real value to our proposition and the performance of our clients. Through our partnerships, our clients can access preferential pricing.
The focus of AKRA TEAM is to support medical device, in-vitro diagnostic and combination device innovators, companies, notified bodies and regulators finding a practical and reasonable approach to fulfill their legal obligations. AKRA TEAM was established to make a difference and ensure that patients receive safe and effective devices in a timely manner.
Developed by practitioners, the ingenious design behind KaizApp blends scientific thinking with mobile technology and an intuitive user experience to enable operational leaders to spend more time coaching and driving results and companies to achieve wider adoption of a performance mindset.
With the most comprehensive set of features on the market, including guided Kaizen, goal tracking and Gemba walks with library, this software is the “Smart A3 meets WhatsApp” for enterprise-wide operational improvement. It accelerates the development of capability, provides visibility of all improvements across your company and makes collaboration easy.
We have developed Smart functionality that augments your own approach to achieve better outcomes
A simple yet powerful ERP/MRP 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 is an accredited training platform designed specifically for pharma, med device and biotech organizations. It provides knowledge and expertise that empowers life science organisations to accelerate growth and remain in an on-going state of compliance.
The 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.
Learnaboutgmp have gone through the rigorous application process for IACET accreditation, to demonstrate the organisation’s commitment to continuing education and training excellence and to ensure students, customers and participants get the best return on their investment.
SoftExpert is a market leader in software for business process improvement and compliance management, to empower organisations to increase business performance at all levels and to maximise industry-mandated compliance and corporate governance programmes.
With 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.
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.
Meddevo sets your focus away from paper documents to content located on local servers or Cloud-based platforms. Manage your technical documentation entirely digitally. Smart Summary Technical Documentation (STED) creates all the necessary documentation for you and monitors its preparedness.
Their dynamic cloud solution fully meets the requirements of the EU Medical Device Regulation (EU MDR 2017/745) and the In-Vitro Diagnostic Regulation (EU 2017/746).
MDlaw, Information Platform on EU Medical Device Regulations offers a system that helps you identify and monitor all the relevant regulatory requirements and changes, as per ISO 13485:2016. MDlaw is the one place where you can find all regulatory documents, guidelines, case-law and updates, gathered and published right after their release.
