In the pharmaceutical industry, where precision, safety, and compliance are non-negotiable, proper document management is critical. From production records and SOPs to compliance documents, every piece of information plays a vital role in ensuring regulatory adherence and product quality. However, […]
Managing documents in the pharmaceutical industry is a complex and critical task. From creation to archival, every document goes through a lifecycle that requires careful handling and strict compliance with regulatory standards. Whether it’s checklists, logbooks, data sheets, or batch […]
In the pharmaceutical industry, keeping your product quality consistent and meeting regulatory standards is essential. The Annual Product Quality Review (APQR) plays a key role in helping you achieve this. By leveraging the best APQR software, you can streamline this […]
What is PQR or APQR in pharma? Annual Product Quality Review or Product Quality Review can be identified as a manoeuvring and compilation of data from various dimensions involved in product manufacturing to display the quality of product. It includes […]
A Document Management System (DMS) is a system used to track, manage and store documents and reduce paper. Most can keep a record of the various versions created and modified by different users. QEdge DMS at a Glance QEdge DMS provides the features and functions […]
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