Sister companies GxP Consulting and Good Products, leading providers of consulting services and electronic Document Management solutions on a SharePoint Platform to the Life Sciences industries, have today announced a merger to form a new company, GxPi. The new company aims to make regulatory compliance simpler for companies within the pharmaceutical, biopharmaceutical and healthcare industries by pairing consultancy services with compliance-based solutions under the company mission to provide products and services that are “Simply Compliant”.
GxPi’s consultancy services will include regulatory compliance, clinical technology, compliant system validation and strategic consulting. The expertise found within GxPi’s consulting arm enables customers to achieve efficient and compliant processes and collaboration across all business functions.
GxPi’s solutions services offer a portfolio of compliance-based products delivered on the x-docs™ platform (formerly g-docs™). The x-docs™ platform is an enhanced ECM SharePoint offering which reduces risk and provides users with compliant document management solutions through packaged validation and pre-defined lifecycle and process management. The x-docs™ product portfolio includes; x-train™ for training management, AdLib for PDF document publication and CoSign® for digital signatures, all of which assist in simplifying the process of regulatory document production and management within the validated environments typically found within Life Science companies.
Keith Williams, CEO, GxPi comments: “We are delighted to announce the merger of Good Products and GxP Consulting and are excited by what this will mean for our business and customers. By combining the two companies we are able to efficiently offer both consultancy services and Document Management solutions to our customers, ensuring compliance for small to medium-sized life science organisations.”
For more information on GxPi, please call +44 (0) 115 924 8477 (EU), +1 949 725 2946 (US), or email info[.]gxpi.com.
GxPi (gxpi.com) provides consultancy services and compliance-based products to the biotechnology, pharmaceutical, consumer healthcare, medical devices and veterinary industries, enabling the development and management of compliant content. The company’s consultancy arm includes high quality, results-focused regulatory compliance (GMP, GAMP, GLP, GEP, GCP, GxP), qualified person (QP), quality assurance (QA), project management, validation, process engineering, computer systems, laboratory equipment, project management, design studies, training and clinical technology consulting services. GxPi also offers Enterprise Content Management (ECM) solutions to the life sciences sector. This provides a new class of document management software which is powerful and practical in enabling sponsors and Contract Research Organisations to comply with increasing regulatory requirements. The solutions are easy to configure, require little IT support, are cost-effective for organisations of all sizes and are entirely intuitive to use with minimal training.