Scientists at a $20B+ pharma giant used Coseer to accelerate drug development by 8X.
Getting KASA-compliant will put you ahead of the curve. It will also make your drug submission process simpler, more transparent, and lead to faster FDA approvals.
Coseer is partnering with leaders in pharma to reimagine clinical trials. Data is getting cleaner, but you have more sources to manage. Let Coseer do the heavy-lifting.
Pharma giants employ 250+ scientists for Adverse Events Compliance. Coseer sifts through millions of documents to extract key data from reports without lifting a finger.
Our customers have been in your shoes.
Only 1 in 5000 drugs make it to market. Coseer accelerates R&D and beats a homegrown solution by 2x in ROI. Tap on the model below.
You search only to get something done. Hover to see how Coseer's NLS enables your workflows.
Collaborate with team members to find answers from data rooms/ repositories and store them in HTML or Word.
Run templated, high-confidence searches to automatically surface all the data points you need.
Program priorities to continuously search your information feeds and get alerts based on preferences.
Automatically find, clean and manage your and your customers' sensitive data.
Ask the right questions in every case and classify things based on the answers you get.
Building internal/ external reports
Structured knowledge management
Real time Intelligence
GDPR/ other Compliance
Scorecard based Classification
Not sure where to start?