IntelliPharma can deliver significant time and cost efficiencies to your organization by helping you throughout the different stages of clinical trials for your pharmaceutical products from the pre-clinical studies phase until the post-marketing surveillance phase. This will help you reduce the startup phase's cost and would assist in meeting the study timelines.
The stakes are higher than ever in clinical research. The clinical development marketplace has become more competitive, while the regulatory standards have become stricter. Our tools can deliver significant time and cost efficiencies while providing better and faster insights.
Improve trial efficiency while lowering costs
Drive healthcare outcomes
Consistent, trusted and verifiable clinical information
Reduced trial process cycle times
Our solution can identify which sites can provide you the required patient pool needed for your clinical trial. This will help you reduce the cost of the start-up phase and also would help in meeting the study timelines.
Our module can help optimize how to target the right locations, qualified investigators, and priority candidates are identified accurately, as well as help analyze the data that is collected more effectively. It can also help to automate workflows by creating drafts of standardized contracts such as confidentiality, investigator, and site agreements to shorten study startup time.
It can also collect and collate evidence that the trial process complies with Good Clinical Practice requirements.
Our clinical Trial Module can help pharmaceutical companies improve patient selection and increase effectiveness.
Our tool mines, analyses, and interprets multiple data sources:
Step 1 - Queries and extracts structured information such as patient demographics and clinical assessments from EHRs,
Step 2 - identifies unstructured information from doctor notes (symptoms, lab values, etc.)
Step 3 - The extracted information is then compared to the eligibility requirements to determine a subject's suitability for a specific clinical trial.
We can help you reshape the critical steps of clinical trial design towards an increased success rate. Our solution can help innovate the trial design by boosting the amount of scientific and research data used:
- Current and past clinical trials.
- Patient support programs
- Post-market surveillance
- Journal papers
- Drug labels
- Other private data owned by the drug or medical device companies
We help you in your Data collection and analysis for your clinical research.
Patients can share data in real-time - they can choose to directly share their information for clinical trials over their mobile devices anywhere and everywhere.
Processing data collected from mobile sensors - AI algorithms, can seamlessly combine with wearable technology, to enable continuous patient monitoring. The data can then undergo immediate analysis, thus improving the response rate.
Research generates a lot of data, and IntelliPharma can help in detecting and interpreting it. Consolidating all the data, whatever the source, through the help of IntelliPharma could help pharma companies determine which indication a drug is more likely to succeed at a much earlier stage.