Activating Data
from Documents

Rethink document processing
drawing of people analyzing a very large document

Stuck

processing documents manually?
Messy documents

If this resonates with you, then Drogevate’s extensible noesis platform and noesis intake may be the right solution for you. Let us help you analyze your situation and help you decide.

noesis framework

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Drawn people standing near lightbulb sign1
Define
Tell us what information you need from your documents
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Rules
Define any business rules to the extracted data
Drawn people using laptop and loudspeaker need talk bubbles sign board3
Specify
Tell us the format of the output you prefer
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Review
Review your defined and mapped outputs
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Process
See your data effortlessly digitized

Where?

Any where you need a form to be digitized
Healthcare
Digitizing forms from Hospitals, ACO’s and Clinics
Hospital plus sign
Clinical
Extracting data from clinical trial forms
Hospital drawing
Safety
Adverse event intake
Shield
Finance
Banking forms, Financial statements and Insurance forms
Coins with plant
Government
Record management systems
Government building
Education
Marksheets, notes to digital content
Books and graduation hat

What makes noesis unique?

  • Any Volume
  • Any Form, Any Language
  • Any output but E2B R2, R3 are standard
  • Any change quickly adopted
  • Not just any accuracy, 95%
  • Insert into any database
6 points what makes drogevate unique

Why noesis?

Innovation
Industry is rapidly seeking innovative solutions, which deliver with precision. Noesis platform's is built using proprietary Data extraction and standardization techniques, infused with Microsoft's Azure blueprint. It is intended to provide industry with a true cloud solution, which enables them to See, Validate and Adapt to latest technologies with a quick turn around and measurable outcome.
Accuracy
Noesis meticulously handles variation of layout in source templates or form, resulting in higher data extraction accuracy.
ROI
Reduced processing times, quickly digitized data at consistently high quality translates to more time in hand for quality review, lower processing cost and increased compliance in regulated environments.

Why Drogevate?

Drogevate brings together a team that has completed scores of successful software development and system implementation projects for Healthcare and Life Sciences industry with a combined experience of 60+ years

We earned our spurs in pharmacovigilance, clinical and regulatory domains. Our passion remains problem solving, developing products and solutions and offer services that fulfill the promises we commit to.

Functional

Successfully designed, developed and deployed global solutions, particularly for Healthcare, Clinical and Pharmacovigilance.

Technology

Successful at implementing high-value, time-sensitive global solutions time and again.

Consulting

Our background includes high-integrity software development for sensitive applications. We apply the best of what that taught us to our software products.

Validation

Meet the Team

Drogevate brings together a team that has completed scores of successful software development and system implementation projects for Pharma. From complex global system implementations to customized solutions we have a combined experience of 60+ years. We earned our spurs in pharmacovigilance, clinical and regulatory domains. Our passion remains problem solving, developing products and solutions that fulfill the promises we commit to.
Founder
Anil Bansal

14 years in incubating, designing, developing and implementing ideas as products and services. He has deep knowledge of various standards such HL7, FHIR, SDTM, SEND, R2, R3 used in healthcare and life sciences domain.

B.E. Gold Medalist from Manipal Institute of Technology, Manipal

Founder
Syed Ali

17+ years of experience in Drug Safety implementations. Is a subject matter expert with expertise in developing integration solutions using ICH E2B and HL7.

B.Tech from Jamia Millia Islamia University, Delhi

Founder
Saurabh Goyal

18+ years of Life Sciences industry experience. In-depth knowledge of various business processes including drug safety, drug development, regulatory submissions and compliance.

MCA from Kurukshetra University, Kurukshetra

VP Strategy
Saeed Amin

20+ years experience leadership roles in Life Sciences quality, IT and data management. In-depth knowledge of program management, drug safety, drug development, regulatory submissions, training and compliance.

B. Comm. (Honours) from University of Ottawa, Canada

Contact

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Everything you need to confidently manage your documents.