Master Production Records (MPR) give the planning department a starting point for determining the materials required for inventory, while Batch Production Records (BPR) consume the inventory during manufacturing. Cutting-edge businesses often store these documents in an Electronic Documentation Management System…
One of the cornerstones of an inventory management system is documentation, such as shipping manifests. Especially in the highly regulated cannabis, pharmaceutical, and biologics industries, generating accurate shipping manifests ensures robust inventory control. Inventory systems often becomes overwhelmed. Inventory teams…
Many companies still use paper-based systems and spreadsheets for their manufacturing documentation despite having numerous solutions available to them. This is in part because companies are concerned about: Process disruption Internal organizational issues Cost Quality system change InstantGMPTM PRO is…
The COVID crisis has done many things, but in particular, it has showcased the vastness and complexity of modern supply chain management. The branches of the modern supply chain extend far and wide, from manufacturing to distribution to allocation of…
Too many virtual biotech companies are working with disjoined systems trying to manage a variety of contractors and vendors. While doing so, they are working to continually fund their manufacturing and clinical activities. To be successful in these efforts, a…
Many customers come to InstantGMP because we provide an efficient way for them to become GMP compliant. After this is accomplished, they want to know how they can become GMP certified. Our partners at the GMP Compliance Resource Center can…
The FDA holds virtual biotech companies accountable for the clinical trials they sponsor. If a problem is to arise during a clinical trial, those who use a quality management system are more easily able to provide the necessary records to…
What is an SOP? Per ICH(International Council on Harmonization), an SOP is a detailed, written instruction to achieve uniformity of the performance of a specific function. They are informed by the guidelines of regulators (FDA, CDPH, etc.) as pertains to…
To succeed today businesses must quickly onboard and train new employees, and simultaneously, keep current employees up-to-date with ever evolving procedures and protocols. As the world of work continues to evolve at record speed, the value of investing in employee…
All cGMP manufacturers are required to keep separate Master Production Records (MPRs) and Batch Production Records (BPRs) in order to comply with FDA regulations. Master Production Records, also known as Master Manufacturing Formulas, are general manufacturing instructions. Each unique formulation…