Success Story: Billev Pharma ApS
"Billev Pharma is working in a very complex environment. In our many years of experience in this field, years of constant development, we have covered most areas of the pharmaceutical sphere, such as: human medicines, veterinary vaccines, herbal medicines, and clinical trial applications. With READY! we are staying at the forefront of finding ways to comprehensively help our clients."
Peter de Mayo Billev, M.Sc. Pharmacy
Get the full story of Billev Pharma Aps 
READY! for Article 57
READY = REgulatory Affairs DiarY
- Regulatory database according to Article 57
- Submission of the data in xEVPRM format
- Regulatory tracking system
- Searching and reporting
- Electronic archive of documents and submissions
- Time and cost tracking
- Services
"READY! for Article 57" is a web-based solution that will enable you to comply to the new Pharmacovigilance regulation. In addition, it is a complete regulatory database and tracking tool, submissions management system, and digital archive of submissions and electronic documents.
READY! will enable you to find information, plan your regulatory activities, prepare comprehensive reports about the status of your regulatory activities, and complete information about your medicinal products.
For more information about Article 57 and XEVMPD, click here.
Are you READY!?