Uncomplicated and Effortless
In today’s everchanging era of Life Science industry, it becomes difficult to gather updated Regulatory information and keep it in accessible format. Information management is a tedious task and Regulatory submissions can be excruciating. Over dependence on file shares with complicated and unreliable sorting methods, electronic mail and tracing databases to oversee your company’s important assets are ineffective, susceptible to errors and they are risky.
Freyr has completely integrated document management and dossier publishing solution that simplifies your Regulatory processes, guarantees compliance and lessens your time to marketplace. Our complete functionality blended with exceptional user functional design consequence with high acceptance rates, accelerating your performances.
Freyr offers industry-proven eCTD publishing, submission and document management software to empower enterprises and efficiently meet all their precise and exceptional Regulatory submission requirements for fast assessments and quicker agreements of their products; Drugs, Biologics and Medical Devices.