Lifesciences Solutions
Taking Lifesciences Companies to a future of open, patient centered, and integrated clinical trials.
Home » Lifesciences Solutions
Life Sciences Solutions
Simply put, our solutions help machines understand medical language and make sense of enormous amounts of unstructured medical data. Science alone cannot fully comprehend disease. This is where Circlebase delivers its innovative use of powerful technologies.
We partner with life science companies and enable them to embrace cloud-based solutions that are powered by AI and leveraged by ML (Machine Learning), NLP (Natural Language Processing), and Machine Vision for efficient health outcomes that advance human health.
AN ALL TOO FAMILIAR SCENARIO
Research teams and investigators are overwhelmed by huge volumes of data every day. This is not surprising, given that over 80% of ALL medical data resides in unstructured form. And they are delivered in every format, including clinical notes, written text, radiology images, pathology slides, video, audio, streaming device data, PDF, emails, faxes, and more.
How does all this impact a life sciences company like yours? Clinical trials’ success depends on data quality, correct interpretation, and correct analytics. The problem for clinical trials today is that they are touched by multiple manual processes, and therefore prone to error. This creates a serious risk for both the patient and overall trial success. Unstructured data capture critical information that impacts every step of good clinical practice for research.
LifeSciences Industry - Key Challenges
High Cost of
Clinical Trials
any delay
Patient Recruitment
Challenges
86%
Frequent Patient
Drop-outs
30%
PRESENTING OUR PORTFOLIO OF SOLUTIONS
Circlebase empowers Life Sciences organizations with our automated solutions to help them make informed decisions to build robust product portfolios, improve R&D productivity and ensure regulatory compliance.
Our solutions unlock the value embedded in data – structured and unstructured – and derive intelligent health outcomes from enormous amounts of data generated.
AI-LED SERVICES FOR EFFICIENT TRIAL
OPERATIONS AND PATIENT-CENTRIC TRIAL DESIGN
NLP LED DATA ENRICHMENT
- Social Determinants of Health (SDOH) data extraction
- Clinical entity extraction: protein, biomarker, etc.
- Chatbots
- Clinical Trial Matching
- Social media analysis
- Medication adherence
Auto coding
(SDTM, ADVERSE EVENTS, AND SERIOUS ADVERSE EVENTS)
- SDTM mapping
- Sample design and automated validation
- Adverse event coding (MedDRA)
- Adverse events cause
- Workflow app for integrating with EDC and auto coding
DRUG DISCOVERY AI
- Analysis of published scientific literature to extract biological knowledge
- Target identification and validation
- Mechanism of Action
- Image analysis (CXR, CT, MRI)
CONTACT CENTER AI/GCP
(SELF HELP, AGENT ASSIST)
- Google Contact Center deployment
- IVR integration
- Skills training for Virtual Agent
- Knowledge Base creation
- Sentiment Analysis from Tone
- Analysis of call recordings for audit
What makes our solutions so compelling? They are designed by a team that has exceptional and highly regarded talent – Data scientists, Natural Language experts, medical data annotation specialists, physicians, and Lifesciences domain experts – whose purpose is to simplify the study process and improve patient outcomes.
CAN A SOLUTION TRULY MAKE A DIFFERENCE?
What excites us about the solutions we have developed is not just the tangible impact on Life sciences Companies and the way they run their business, but the impact it has on the lives of patients – making their lives more pleasant and less stressful. Read on to see the many benefits we offer:
But as with any solution, it is only as good as its knowledge base, which is why we don’t stop with its development, rather we continuously train the model for improved accuracy. The result? Efficient results, significant reduction in clinical trial costs and trial duration, but most importantly, increased success rate of your trials.
Our Value Proposition
- Restart and accelerate your trials
- Embrace remote trials
- Increase your chances of FDA approvals through accurate submission of data
- Improve process efficiency and reliability (>95% accuracy)
- Reduce adverse events and better risk identification