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Pharmaceutical companies and regulatory agencies use our software to get rid of all those Excel spreadsheets, outdated regulatory databases, and paper-based documents.
Instead of unproductive time spent populating Excels, users of READY! can focus on their scientific work.
This translates into more work done with less stress.
Outstanding services
Our experts have many years of experience and a deep understanding of processes in the pharmaceutical industry.
We are proud that our annual Customer Satisfaction Survey demonstrates total satisfaction with our services, from implementation to support.
All of our projects have been successful and finished within the agreed-upon time and price.
Innovative products
The Pharma industry is one of the most regulated, which results in complex processes and huge resources spent on tracking and documenting product-related information.
We have cracked this problem and developed innovative software that significantly reduces the resources and the time needed to meet all regulatory requirements.
READY! is web-based and is built on ISO IDMP standards, including support for Article 57/HL7 submissions.
READY! comprises integrated software products:
- 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! SOLUTIONS
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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Replace Excel spreadsheets, shared drives, and outdated regulatory databases.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.
