Backed by
Regulatory AI Agents
for Lifescience
Entvin AI is an intelligent agent platform which streamline FDA compliance for regulatory, medical affairs and commercial teams.
Trusted by regulatory and pharma professionals from
world’s leading organisations
Problem
Navigating Pharma Data is a Struggle
Today's pharma teams are overwhelmed by fragmented data, regulatory hurdles, and time-consuming processes that slow down innovation
Fragmented Regulatory Databases:
Regulatory teams struggle with siloed datasets from multiple sources like FDA PIL, SBOA review documents, PSG, IIG Database, and global regulatory databases (Drugs@FDA, EMA, TGA), making data retrieval and dossier preparation cumbersome and time-intensive.
Manual Data Extraction from Regulatory Submissions:
Regulatory teams spend countless hours extracting and analyzing data from regulatory documents, and market submissions, reducing efficiency and accuracy in regulatory filings.
Unstructured Data and Lack of Insights:
Regulatory teams struggle with siloed datasets from multiple sources like FDA PIL, SBOA review documents, PSG, IIG Database, and global regulatory databases (Drugs@FDA, EMA, TGA), making data retrieval and dossier preparation cumbersome and time-intensive.
17
Sunday
18
Monday
19
Tuesday
20
Wednesday
21
Thursday
22
Friday
23
Saturday
24
Sunday
You missed the new FDA regulatory update published 2 days ago
New Regulatory Update
from FDA
2 days ago
🤯
I can’t afford to miss such
updates next time!
Navigating Evolving Regulatory Landscapes:
Keeping up with constantly changing submission requirements, compliance policies, and country-specific regulations is a major hurdle, increasing the risk of rejections, costly delays, and non-compliance penalties.
Formulation Development Report
Project Title: Novel Tablet Formulation for Extended Release of
XYZ Compound
Date: November 18, 2024
Formulation Scientist: Dr. Alex Johnson
1. Introduction
Objective:
Batch Results:
Batch
Hypromellose
(%)
Dissolution
Time (hrs)
Assay (%)
Stability
Observations
F1
4
98.5
Stable
5
To develop an extended-release tablet formulation of XYZ compound that meets desired pharmacokinetic (PK) parameters and achieves targeted therapeutic levels.
The regulatory team wants
the data in a different
format.
Manual Regulatory Report and Label Drafting:
Drafting regulatory reports, prescribing information, and product labels manually requires extensive effort and cross-functional coordination. Errors in labeling or documentation can lead to compliance issues, submission delays, and potential regulatory rejections.
Solution
Meet
Your AI Copilot for Pharma Intelligence
Unlock instant, data-driven insights to help pharma professionals drive innovation, ensure compliance, and make strategic decisions at the right time.
Retrieve
Analyze
Report
Centralized Data Integration:
Access siloed datasets from FDA, EMA, TGA, and more in one unified platform.
Instant Access to Regulatory Documents:
Retrieve critical documents like FDA PIL, SBOA review documents, PSG, and IIG Database instantly.
Custom Alerts and Notifications:
Set intelligent alerts on regulatory updates and market changes.
Teams
Your AI Copilot, Tailored for Every Team
Explore how our AI Copilot empowers your team by addressing their unique needs and answering their most pressing questions. From strategy to execution, discover the possibilities designed to transform the way you work.
R&D, Formulation,
& Analytical Teams
Regulatory Affairs Team
Portfolio &
Commercial Teams
What are the most common excipients used in similar drugs for specific indications?
What dissolution profiles should be expected based on similar formulations?
How can historical data help improve my formulation’s chances for faster approval?
Security
Modern Enterprise Grade Data Security
That Pharma Needs
Your data is protected with advanced security measures, ensuring privacy and reliability at every step.
Hyper-Secure Deployment
Hosted securely in a dedicated private cloud environment.
Hyper-Secure Deployment
Hosted securely in a dedicated private cloud environment.
Regulatory Compliance
Certified with SOC2, ISO, HIPAA, and GDPR standards, with regular audits.
Regulatory Compliance
Certified with SOC2, ISO, HIPAA, and GDPR standards, with regular audits.
Secure User Data
Ensures robust security for user activity logs and data, preserving confidentiality and integrity
Secure User Data
Ensures robust security for user activity logs and data, preserving confidentiality and integrity
Testimonials
Insights and Stories
from Innovators Driving Change
As a scientist working on complex generics, I'm impressed by Entvin's comprehensive approach. Their tool not only pulls critical parameters from various regulatory and scientific documents but also provides AI-generated insights on excipient compatibility and dissolution methods. This level of analysis typically takes our team weeks to compile manually.
Scientist
Formulation Development
Entvin provides a comprehensive overview of critical RLD parameters by intelligently extracting data from multiple regulatory sources. This level of automation and insight is invaluable for FR&D scientists looking to accelerate their development process.
Scientist
Formulation Development
Entvin's R&D assistant dramatically reduces the time spent searching through regulatory documents, allowing scientists to focus more on lab work and FR&D.
Director
Formulation Development
As a scientist working on complex generics, I'm impressed by Entvin's comprehensive approach. Their tool not only pulls critical parameters from various regulatory and scientific documents but also provides AI-generated insights on excipient compatibility and dissolution methods. This level of analysis typically takes our team weeks to compile manually.
Scientist
Formulation Development
Entvin provides a comprehensive overview of critical RLD parameters by intelligently extracting data from multiple regulatory sources. This level of automation and insight is invaluable for FR&D scientists looking to accelerate their development process.
Scientist
Formulation Development
Entvin's R&D assistant dramatically reduces the time spent searching through regulatory documents, allowing scientists to focus more on lab work and FR&D.
Director
Formulation Development
"As a scientist working on biologics, I'm impressed by Entvin's comprehensive approach to aggregating regulatory data. Their AI assistant that can rapidly extract key details from lengthy documents is particularly valuable. With some enhancements to include more peer-reviewed scientific sources, this platform could become an indispensable tool for formulation scientists across the industry.”
Scientist
Formulation Development
Entvin has developed an innovative solution that addresses a critical need in the pharmaceutical industry. Their AI-driven approach to literature review is not only time-saving but also provides insights that could lead to more efficient drug development processes. It's exciting to see how this technology could shape the future of pharmaceutical research.
Scientist
Formulation Development
"As a scientist working on biologics, I'm impressed by Entvin's comprehensive approach to aggregating regulatory data. Their AI assistant that can rapidly extract key details from lengthy documents is particularly valuable. With some enhancements to include more peer-reviewed scientific sources, this platform could become an indispensable tool for formulation scientists across the industry.”
Scientist
Formulation Development
Entvin has developed an innovative solution that addresses a critical need in the pharmaceutical industry. Their AI-driven approach to literature review is not only time-saving but also provides insights that could lead to more efficient drug development processes. It's exciting to see how this technology could shape the future of pharmaceutical research.
Scientist
Formulation Development
Contact us
Stay Ahead in Pharma Innovation
Allow Entvin AI to bear the burden, delivering the key insights necessary for promoting swift decision-making. Plan your demonstration now!
FAQs
Got Questions?
We've Got Answers!
How does Entvin ensure compliance with regulatory standards?
Entvin ensures compliance with industry-leading regulatory standards by adhering to rigorous frameworks such as SOC 2 TYPE 2, ISO 27001, GDPR, and HIPAA. These certifications and frameworks ensure that data privacy, security, and compliance are maintained throughout our platform, safeguarding sensitive information and meeting the highest standards in the industry. This allows our users to trust that their data is managed in accordance with the most stringent regulatory requirements.
How does Entvin ensure compliance with regulatory standards?
Entvin ensures compliance with industry-leading regulatory standards by adhering to rigorous frameworks such as SOC 2 TYPE 2, ISO 27001, GDPR, and HIPAA. These certifications and frameworks ensure that data privacy, security, and compliance are maintained throughout our platform, safeguarding sensitive information and meeting the highest standards in the industry. This allows our users to trust that their data is managed in accordance with the most stringent regulatory requirements.
How does Entvin ensure the accuracy of its insights?
How does Entvin ensure the accuracy of its insights?
How does Entvin automate and streamline drug data analysis?
How does Entvin automate and streamline drug data analysis?
Can I get daily updates on new data added to the platform?
Can I get daily updates on new data added to the platform?
What pricing models does Entvin offer?
What pricing models does Entvin offer?
USA
1111B S Governors Ave STE 6003 Dover, DE 19904
India
Entvin Labs Pvt. Ltd. No 351 Salarpuria Towers-I, Hosur Road, Koramangala, Bengaluru, Karnataka, India- 560095
Backed by
© Entvin, Inc. 2024 — All rights reserved.
Backed by
AI Copilot
for Pharma Intelligence
Entvin AI empowers pharma companies with AI-powered research with regulatory drug databases like FDA, EMA, TGA
Trusted by
Problem
Navigating Pharma Data is a Struggle
Today's pharma teams are overwhelmed by fragmented data, regulatory hurdles, and time-consuming processes that slow down innovation
Manual Data Extraction and Analysis:
Extracting and analyzing data from regulatory documents and clinical trial reports remains a slow and
error-prone process that limits efficiency and accuracy.
Manual Data Extraction and Analysis:
Extracting and analyzing data from regulatory documents and clinical trial reports remains a slow and
error-prone process that limits efficiency and accuracy.
Unstructured Data and Lack of Insights:
Unstructured data from clinical trials, regulatory submissions, and market reports hinders actionable insights for decision-making.
Unstructured Data and Lack of Insights:
Unstructured data from clinical trials, regulatory submissions, and market reports hinders actionable insights for decision-making.
Formulation Development Report
Project Title: Novel Tablet Formulation for Extended Release of
XYZ Compound
Date: November 18, 2024
Formulation Scientist: Dr. Alex Johnson
1. Introduction
Objective:
Batch Results:
Batch
Hypromellose
(%)
Dissolution
Time (hrs)
Assay (%)
Stability
Observations
F1
4
98.5
Stable
5
To develop an extended-release tablet formulation of XYZ compound that meets desired pharmacokinetic (PK) parameters and achieves targeted therapeutic levels.
The regulatory team wants
the data in a different
format.
Manual Report Drafting
Time-consuming manual report creation hinders efficiency in capturing and analyzing formulation data, slowing down decision-making in critical research workflows.
Data Overload and Fragmented Information:
R&D and Regulatory Affairs teams spend too much time navigating siloed data sources, like FDA, EMA and TGA, to find relevant insights.
Data Overload and Fragmented Information:
R&D and Regulatory Affairs teams spend too much time navigating siloed data sources, like FDA, EMA and TGA, to find relevant insights.
17
Sunday
18
Monday
19
Tuesday
20
Wednesday
21
Thursday
22
Friday
23
Saturday
24
Sunday
You missed the new FDA regulatory update published 2 days ago
New Regulatory Update
from FDA
2 days ago
🤯
I can’t afford to miss such
updates next time!
Complex and Constantly Changing Regulatory Landscape:
Adapting to changing regulations is challenging, risking delays or lost approvals.
Security
Modern Enterprise Grade Data Security That Pharma Needs
Your data is protected with advanced security measures, ensuring privacy and reliability at every step.
Manual Data Extraction and Analysis:
Extracting and analyzing data from regulatory documents and clinical trial reports remains a slow and
error-prone process that limits efficiency and accuracy.
Manual Data Extraction and Analysis:
Extracting and analyzing data from regulatory documents and clinical trial reports remains a slow and
error-prone process that limits efficiency and accuracy.
Unstructured Data and Lack of Insights:
Unstructured data from clinical trials, regulatory submissions, and market reports hinders actionable insights for decision-making.
Unstructured Data and Lack of Insights:
Unstructured data from clinical trials, regulatory submissions, and market reports hinders actionable insights for decision-making.
Formulation Development Report
Project Title: Novel Tablet Formulation for Extended Release of
XYZ Compound
Date: November 18, 2024
Formulation Scientist: Dr. Alex Johnson
1. Introduction
Objective:
Batch Results:
Batch
Hypromellose
(%)
Dissolution
Time (hrs)
Assay (%)
Stability
Observations
F1
4
98.5
Stable
5
To develop an extended-release tablet formulation of XYZ compound that meets desired pharmacokinetic (PK) parameters and achieves targeted therapeutic levels.
The regulatory team wants
the data in a different
format.
Manual Report Drafting
Time-consuming manual report creation hinders efficiency in capturing and analyzing formulation data, slowing down decision-making in critical research workflows.
Data Overload and Fragmented Information:
R&D and Regulatory Affairs teams spend too much time navigating siloed data sources, like FDA, EMA and TGA, to find relevant insights.
Data Overload and Fragmented Information:
R&D and Regulatory Affairs teams spend too much time navigating siloed data sources, like FDA, EMA and TGA, to find relevant insights.
17
Sunday
18
Monday
19
Tuesday
20
Wednesday
21
Thursday
22
Friday
23
Saturday
24
Sunday
You missed the new FDA regulatory update published 2 days ago
New Regulatory Update
from FDA
2 days ago
🤯
I can’t afford to miss such
updates next time!
Complex and Constantly Changing Regulatory Landscape:
Adapting to changing regulations is challenging, risking delays or lost approvals.
Solution
Meet
Your AI Copilot for Pharma Intelligence
Unlock instant, data-driven insights to help pharma professionals drive innovation, ensure compliance, and make strategic decisions at the right time.
Retrieve
Analyze
Report
Centralized Data Integration:
Access siloed datasets from FDA, EMA, TGA, and more in one unified platform.
Instant Access to Regulatory Documents:
Retrieve critical documents like FDA PIL, SBOA review documents, PSG, and IIG Database instantly.
Real-Time Market Data:
Stay updated with real-time data from drug databases.
Solution
Meet
Your AI Copilot for Pharma Intelligence
Unlock instant, data-driven insights to help pharma professionals drive innovation, ensure compliance, and make strategic decisions at the right time.
Retrieve
Analyze
Report
Centralized Data Integration:
Access siloed datasets from FDA, EMA, TGA, and more in one unified platform.
Instant Access to Regulatory Documents:
Retrieve critical documents like FDA PIL, SBOA review documents, PSG, and IIG Database instantly.
Real-Time Market Data:
Stay updated with real-time data from drug databases.
Teams
Your AI Copilot, Tailored for Every Team
Explore how our AI Copilot empowers your team by addressing their unique needs and answering their most pressing questions. From strategy to execution, discover the possibilities designed to transform the way you work.
R&D, Formulation,
& Analytical Teams
Regulatory Affairs Team
Portfolio &
Commercial Teams
What are the most common excipients used in similar drugs for specific indications?
What dissolution profiles should be expected based on similar formulations?
How can historical data help improve my formulation’s chances for faster approval?
Teams
Your AI Copilot, Tailored for Every Team
Explore how our AI Copilot empowers your team by addressing their unique needs and answering their most pressing questions. From strategy to execution, discover the possibilities designed to transform the way you work.
R&D, Formulation,
& Analytical Teams
Regulatory Affairs Team
Portfolio &
Commercial Teams
What are the most common excipients used in similar drugs for specific indications?
What dissolution profiles should be expected based on similar formulations?
How can historical data help improve my formulation’s chances for faster approval?
Contact us
Stay Ahead in Pharma Innovation
Let Entvin AI do the heavy lifting, providing the insights you need to
drive faster decisions. Schedule your demo today!
FAQs
Got Questions?
We've Got Answers!
How does Entvin ensure compliance with regulatory standards?
Entvin ensures compliance with industry-leading regulatory standards by adhering to rigorous frameworks such as SOC 2 TYPE 2, ISO 27001, GDPR, and HIPAA. These certifications and frameworks ensure that data privacy, security, and compliance are maintained throughout our platform, safeguarding sensitive information and meeting the highest standards in the industry. This allows our users to trust that their data is managed in accordance with the most stringent regulatory requirements.
How does Entvin ensure the accuracy of its insights?
How does Entvin automate and streamline drug data analysis?
Can I get daily updates on new data added to the platform?
What pricing models does Entvin offer?
FAQs
Got Questions?
We've Got Answers!
How does Entvin ensure compliance with regulatory standards?
Entvin ensures compliance with industry-leading regulatory standards by adhering to rigorous frameworks such as SOC 2 TYPE 2, ISO 27001, GDPR, and HIPAA. These certifications and frameworks ensure that data privacy, security, and compliance are maintained throughout our platform, safeguarding sensitive information and meeting the highest standards in the industry. This allows our users to trust that their data is managed in accordance with the most stringent regulatory requirements.
How does Entvin ensure the accuracy of its insights?
How does Entvin automate and streamline drug data analysis?
Can I get daily updates on new data added to the platform?
What pricing models does Entvin offer?
USA
1111B S Governors Ave STE 6003 Dover, DE 19904
India
Entvin Labs Pvt. Ltd. No 351 Salarpuria Towers-I,
Hosur Road, Koramangala, Bengaluru,
Karnataka, India- 560095
Backed by
© Entvin, Inc. 2024 — All rights reserved.
Backed by
AI Copilot
for Pharma Intelligence
Entvin AI empowers pharma companies with
AI-powered research with regulatory drug databases like FDA, EMA, TGA
Get Started
Trusted by
Problem
Navigating Pharma Data is a Struggle
Today's pharma teams are overwhelmed by fragmented data, regulatory hurdles, and time-consuming processes that slow down innovation
Manual Data Extraction and Analysis:
Extracting and analyzing data from regulatory documents and clinical trial reports remains a slow and error-prone process that limits efficiency and accuracy.
Manual Data Extraction and Analysis:
Extracting and analyzing data from regulatory documents and clinical trial reports remains a slow and error-prone process that limits efficiency and accuracy.
Unstructured Data and Lack of Insights:
Unstructured data from clinical trials, regulatory submissions, and market reports hinders actionable insights for decision-making.
Unstructured Data and Lack of Insights:
Unstructured data from clinical trials, regulatory submissions, and market reports hinders actionable insights for decision-making.
Data Overload and Fragmented Information:
R&D and Regulatory Affairs teams spend too much time navigating siloed data sources, like FDA, EMA and TGA, to find relevant insights.
Data Overload and Fragmented Information:
R&D and Regulatory Affairs teams spend too much time navigating siloed data sources, like FDA, EMA and TGA, to find relevant insights.
Formulation Development Report
Project Title: Novel Tablet Formulation for Extended Release of
XYZ Compound
Date: November 18, 2024
Formulation Scientist: Dr. Alex Johnson
1. Introduction
Objective:
Batch Results:
Batch
Hypromellose
(%)
Dissolution
Time (hrs)
Assay (%)
Stability
Observations
F1
4
98.5
Stable
5
To develop an extended-release tablet formulation of XYZ compound that meets desired pharmacokinetic (PK) parameters and achieves targeted therapeutic levels.
The regulatory team
wants the data in a
different format.
Manual Report Drafting
Time-consuming manual report creation hinders efficiency in capturing and analyzing formulation data, slowing down decision-making in critical research workflows.
Complex and Constantly Changing Regulatory Landscape:
Adapting to changing regulations is challenging, risking delays or lost approvals.
Security
Modern Enterprise Grade Data Security
That Pharma Needs
Your data is protected with advanced security measures, ensuring privacy and reliability at every step.
Hyper-Secure Deployment
Hosted securely in a dedicated private cloud environment.
Hyper-Secure Deployment
Hosted securely in a dedicated private cloud environment.
Regulatory Compliance
Certified with SOC2, ISO, HIPAA, and GDPR standards, with regular audits.
Regulatory Compliance
Certified with SOC2, ISO, HIPAA, and GDPR standards, with regular audits.
Secure User Data
Ensures robust security for user activity logs and data, preserving confidentiality and integrity
Secure User Data
Ensures robust security for user activity logs and data, preserving confidentiality and integrity
Solution
Meet
Your AI Copilot for Pharma Intelligence
Unlock instant, data-driven insights to help pharma professionals drive innovation, ensure compliance, and make strategic decisions at the right time.
Retrieve
Analyze
Report
Centralized Data Integration:
Access siloed datasets from FDA, EMA, TGA, and more in one unified platform.
Instant Access to Regulatory Documents:
Retrieve critical documents like FDA PIL, SBOA review documents, PSG, and IIG Database instantly.
Real-Time Market Data:
Stay updated with real-time data from drug databases.
Solution
Meet
Your AI Copilot for Pharma Intelligence
Unlock instant, data-driven insights to help pharma professionals drive innovation, ensure compliance, and make strategic decisions at the right time.
Retrieve
Analyze
Report
Centralized Data Integration:
Access siloed datasets from FDA, EMA, TGA, and more in one unified platform.
Instant Access to Regulatory Documents:
Retrieve critical documents like FDA PIL, SBOA review documents, PSG, and IIG Database instantly.
Real-Time Market Data:
Stay updated with real-time data from drug databases.
Teams
Your AI Copilot, Tailored for Every Team
Explore how our AI Copilot empowers your team by addressing their unique needs and answering their most pressing questions. From strategy to execution, discover the possibilities designed to transform the way you work.
R&D, Formulation,
& Analytical Teams
Regulatory Affairs Team
Portfolio &
Commercial Teams
What are the most common excipients used in similar drugs for specific indications?
What dissolution profiles should be expected based on similar formulations?
How can historical data help improve my formulation’s chances for faster approval?
Teams
Your AI Copilot, Tailored for Every Team
Explore how our AI Copilot empowers your team by addressing their unique needs and answering their most pressing questions. From strategy to execution, discover the possibilities designed to transform the way you work.
R&D, Formulation,
& Analytical Teams
Regulatory Affairs Team
Portfolio &
Commercial Teams
What are the most common excipients used in similar drugs for specific indications?
What dissolution profiles should be expected based on similar formulations?
How can historical data help improve my formulation’s chances for faster approval?
Contact us
Stay Ahead in Pharma Innovation
Let Entvin AI do the heavy lifting, providing the insights you need to drive faster decisions. Schedule your demo today!
How does Entvin ensure compliance with regulatory standards?
How does Entvin ensure the accuracy of its insights?
How does Entvin automate and streamline drug data analysis?
Can I get daily updates on new data added to the platform?
What pricing models does Entvin offer?
FAQs
Got Questions?
We've Got Answers!
How does Entvin ensure compliance with regulatory standards?
How does Entvin ensure the accuracy of its insights?
How does Entvin automate and streamline drug data analysis?
Can I get daily updates on new data added to the platform?
What pricing models does Entvin offer?
FAQs
Got Questions?
We've Got Answers!
USA
1111B S Governors Ave STE 6003 Dover, DE 19904
India
Entvin Labs Pvt. Ltd. No 351 Salarpuria Towers-I,
Hosur Road, Koramangala, Bengaluru,
Karnataka, India- 560095
Backed by
© Entvin, Inc. 2024 — All rights reserved.