Developing a pharmaceutical drug is a long, difficult & pain staking process. The process usually involves a pre-trial phase, a clinical trial phase & a commercialisation or product launch phase for every drug a pharmaceutical company develops. All these processes require accurate & timely documentation, like maintaining documents on the drug’s development, information on the research team, funding records, animal & human trial studies, drug composition, regulatory compliances, and much more. Delays in development & approval of these documents can result in losses amounting to billions of dollars for the company. That is why many pharma companies across the world have switched to GLOBODOX document management software, to manage all their documents & business correspondence at one place. GLOBODOX document management system helps pharmaceutical companies maintain an accurate log of the drug’s entire life cycle – from pre-trial to marketing, accelerates document approvals & transfers, improves data security, and helps drug manufacturers comply with regulatory protocols like good laboratory practices (GLP), current goods manufacturing processes (cGMP) & other health, safety & data security guidelines issued by the FDA. Here is how GLOBODOX transforms the document & information management processes for pharmaceutical or biotechnology companies: