R programming in clinical trials- Genpro

1
Our Products - R programming in clinical trials

• Our products use AI in clinical trials , Machine
  Learning Natural Language Processing to
  automate some of the time-consuming manual
  processes involved in clinical research, drug and
  device development, and various stages of product
  life cycle. Systematic Literature Review,
  Clinical Data visualization Data Submissions
  are automated using these tools to help
  organisations to increase their productivity by
  50 70.

2

• Automating Medical Scientific Literature
  Search, Review Authoring
• Voody is a semi-automated platform that enables
  the researchers to search, filter, author,
  review, and publish scientific and medical
  documents. Voodys machine-assisted document
  processing and information extraction combined
  with seamless integration of PubMed reduce
  cognitive overload for researchers up to 70.
  Voodys automated information source citing and
  linking to the context document eases the review
  process for researchers. Integrated QC module in
  VOODY provides fast and easy validation of the
  document before publishing. Voody also provides a
  single searchable repository of all the documents
  that are produced through this process.

3

• NLP Based Clinical Data Visualization
• MOSS is a clinical data analysis and
  visualisation tool which makes use of Natural
  Language Processing and Deep Learning algorithms
  to automatically translate a natural language
  (English) question from a clinician to a
  structured database query. MOSS will then render
  the output in an aesthetically appealing form
  (charts, graphs, tables, tokens) and will also
  allow drill down analysis on these reports. MOSS
  allows clinicians and trial monitors to reduce
  their dependence on the data team to do ad-hoc
  visualisations and analysis of key risk
  indicators. MOSS will also provide statistical
  analysis plugins in future releases so that the
  clinicians will be able to perform basic data
  analysis.

4

• Data Submission Simplified
• SUBX is an intelligent submission tool developed
  by Genpro that help sponsors to better prepare
  for their NDA/PMDA submissions. As Sponsor is
  preparing for their NDA submission, it is
  critical for them to verify the content and
  validity of the dataset folder per the FDA
  submission requirements. Datasets must meet the
  technical specifications per the Study Data TCG
  and eCTD validation criteria. Our submission
  validation framework will check whether the
  datasets that are provided for regulatory
  publishing is compliant to the FDA/EMEA guidance.

5
Our Mission

• Our mission is to support our clients in
  achieving their goals by providing knowledge
  driven innovative solutions with highest quality
  products and services.
• WHO WE ARE
• Genpro Research is a next-generation services and
  technology partner for the pharmaceutical,
  biotechnology, and medical devices industry. Our
  tools use AI in clinical trials , Statistical
  Programming services, Machine Learning, and
  Natural Language Processing algorithms to enable
  automation of several processes in a drug
  development pipeline.. We provide advanced
  solutions in Biostatistics Programming, Medical
  Writing, and Regulatory Submissions.

6
GET IN TOUCH WITH US Follow Us On Social
Networks Facebook Twitter LinkedIn C