About us
For more than 15 years, our sole focus has been the design, implementation, and validation of innovative software solutions for the pharmaceutical industry.
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companies and regulatory agencies rely on our software to eliminate the need for cumbersome Excel spreadsheets, outdated regulatory databases, and paper-based documents.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 document searching, allowing them to concentrate on their scientific work.
This transition translates into increased productivity with reduced stress.
Outstanding services
Our experts have many years of experience and a deep understanding of processes in the pharmaceutical industry.
We take pride in the outcomes of our annual Customer Satisfaction Survey, which consistently reflects total satisfaction with our services, spanning from implementation to support.
Moreover, every one of our projects has achieved success, consistently meeting both the agreed-upon timelines and budgets.
Innovative software products
The pharmaceutical industry is one of the most highly regulated, leading to complex processes and substantial resource allocation for tracking and documenting product-related information.
We’ve tackled this issue by developing innovative software that dramatically reduces the resources and time required to meet all regulatory requirements.
READY! is web-based and is built on ISO IDMP standards, including support for Article 57/HL7 submissions.
READY! provides integrated functionality:
- Product database and activity tracking
- Document management and dossier compilation
- ISO IDMP/Article 57 reporting gateway
READY! replaces all those Excel spreadsheets and shared drives.
Proud sponsor of our local volleyball team!
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Replace Excel spreadsheets, shared drives, and outdated regulatory databases.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 the pharmaceutical industry.
