Our focus
Within the pharmaceutical industry, the integrity of documents and data plays a crucial role, both during the development phase and in ensuring the ongoing quality and safety of products once they are in use.
Pharmaceutical companies and regulatory agencies rely on our software to eliminate the need for cumbersome Excel spreadsheets, outdated regulatory databases, and paper-based documents.
With READY!, users can redirect their valuable time away from data entry and Excel sheets, allowing them to focus on their scientific work.
This transition translates into increased productivity with reduced stress.
READY! CONFIGURATIONS
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READY! for ePI
Prepare, submit, and maintain documents in ePI with our pre-configured READY! platform.
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Product information, Labelling
Increase efficiency in the approval of PI during regulatory procedures.
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Regulatory Affairs
Replace Excel spreadsheets, shared drives, and outdated regulatory databases.
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Article 57 reporting gateway
Exchange medicinal product information with a click on one button.
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Pharmacovigilance
Promote, maintain, and improve compliance with the legal requirements.
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Development
Track milestones and store documents created in the development of a new medicine.
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Quality Assurance
Manage processes, documents, and products in one integrated platform.
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Are you READY! ?
Manage product information, safety data, and documents in one validated environment.
READY! stands for: REgulated Affairs DiarY
READY! is based around the idea that companies need updated, current information about their products in all of their iterations.
READY! has been developed to meet specific needs of management of structured (IDMP medicinal product information) and unstructured information (documents, forms, records) in pharma industry.
