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Companies that work with a host of vendors and suppliers know just how complex and essential their supply chain is. It is imperative that each connection with a vendor or supplier is documented in a formalized system. The data in those documents is...
Managing packaging specifications can be a tedious process, especially in highly regulated companies. Being part of the pharmaceutical industry requires careful management of thousands of complex specifications and strict adherence to many...
Tags: Packaging Management Software, pharmaceutical, regulatory, packaging specification management software
Patrick Crowley is one of DocXellent’s Technical Support Engineers, a proud Jiu-Jitsu competitor, and our company’s “Mr. Migration”! As a technical support engineer at DocXellent, he has the responsibility of software installations for our...
Tags: ENSUR Document Management, employee spotlight, DocXellent Employees, data migration
As technology becomes more and more advanced, companies across the globe that manufacture products or design packaging have begun moving away from manual, paper processes and are opting for electronic specification management systems. Optimizing...
Tags: specification management, cyber security, managed cloud, sustainability
A Document Management System (DMS) allows your company to move from an inefficient paper process to a digital one that will cut costs and improve your data security – when done properly. Whether you are new to the DMS realm or have been using one...
Tags: document management system, automated workflow, document management software company, regulatory
Packaging materials and labor can be costly for companies who package products. Managing the various types of packaging components and materials in an efficient and controlled way can prevent issues with timelines, costs, customer loyalty, and even...
Preparing for an ISO audit is a necessary and complicated aspect of operating within a highly regulated industry. It is the job of the auditor to make sure all of your documentation and processes are running in line with every ISO regulation....
Tags: quality management, quality management process, ISO 9001, audit
A Certificate of Analysis (COA) is a document that manufacturers produce that verifies the product they manufactured conforms to their customer’s requirements. It is important for the customers to know that the product they are receiving adheres to...
Tags: Document Management Systems, certificate of analysis, COA
Artificial Intelligence (AI) and machine learning are the newest technologies revolutionizing the medical device industry. These advances have the potential to transform the way medical device companies gather important insights from the vast...
Tags: FDA compliance software, medical device document control, AI, Artificial Intelligence, medical device