The pharmaceutical biotech industry generates massive amount of paper files from clinical studies, New Drug Applications (NDA's), Investigational New Drug (IND's), disease diagnostics, drug discovery, quality control etc.. Doing business faster, smarter, and easier is a business-intelligence need for the biotech industry. Document retention is one of many keys FDA compliances regulating the pharmaceutical industry. Govitec helps businesses answering compliance and business-intelligence purposes by converting/processing
- Clinical Studies,
- New Drug Applications (NDA's)
- Investigational New Drug (IND's)
- Disease Diagnostics
- Drug Discovery fles
- Quality control files
Into images while boosting throughput, reliability, data dictionary and taxonomy validation and reproducibility.
Document conversion has the benefits of increasing productivity, performance, and profit in allowing subject matter experts quicker access to information.
Govitec has performed various onsite and offsite conversions (ABIC, AFP, JBIG, JPEG, MO:DCA, MS Word, MS Excel, PCL, PDF, PDF/A, and TIFF) into known imaging systems such as documentum, onbase.
Govitec is committed to deliver powerful, flexible, and reliable imaging solutions to the pharmaceutical industry.