Safety & Pharmacovigilance

lmprove patient safety, optimize global compliance, and make better decisions faster.

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Safety & Pharmacovigilance

Our solution accelerator built 100% native on Salesforce Service Cloud offers 360 degree view across R&D and commercial and helps enable pharma, bio-tech and medical devices companies to make faster and better safety decisions, optimize global compliance and easily integrate risk management.

Product Features

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Analytics & Reporting

Analytics & Reporting functionality helps in developing striking, vibrant reports for C-suite executives and end-users to understand insights regarding the operations of a day with bundled reports.

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Medwatch Information

Users could easily enter the additional information required in the MedWatch 3500A report with Cloudbyz platform and develop the report immediately and filing it electronically without leaving system.

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Medwatch Information

Users could easily enter the additional information required in the MedWatch 3500A report with Cloudbyz platform and develop the report immediately and filing it electronically without leaving system.

Case Management

Cloudbyz enables resilient processes with higher scalability and end-to-end safety process with global case processing, E2B intake and submission, periodic reporting and other activities.

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Adverse Event Management

The solutions for collaborative, user-oriented and detailed periodic reporting of adverse events with PSUR, PADER, ASR, DSUR and others help in faster routine submissions with better accuracy.

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Adverse Event Management

The solutions for collaborative, user-oriented and detailed periodic reporting of adverse events with PSUR, PADER, ASR, DSUR and others help in faster routine submissions with better accuracy.

Product Management

Product management functionality can improve safety & pharmacovigilance solution by recording and managing details regarding products and dosage regimens while building associations for data accuracy.

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Event Analysis

Events analysis functionality helps in creating or reviewing narrative description of cases along with other notes and data for all system events with support for regulatory report information input.

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Event Analysis

Events analysis functionality helps in creating or reviewing narrative description of cases along with other notes and data for all system events with support for regulatory report information input.

Product Features

Analytics & Reporting

Analytics & Reporting functionality helps in developing striking, vibrant reports for C-suite executives and end-users to understand insights regarding the operations of a day with bundled reports.

Medwatch Information

Users could easily enter the additional information required in the MedWatch 3500A report with Cloudbyz platform and develop the report immediately and filing it electronically without leaving system.

Case Management

Cloudbyz enables resilient processes with higher scalability and end-to-end safety process with global case processing, E2B intake and submission, periodic reporting and other activities.

Adverse Event Management

The solutions for collaborative, user-oriented and detailed periodic reporting of adverse events with PSUR, PADER, ASR, DSUR and others help in faster routine submissions with better accuracy.

Adverse Event Management

The solutions for collaborative, user-oriented and detailed periodic reporting of adverse events with PSUR, PADER, ASR, DSUR and others help in faster routine submissions with better accuracy.

Product Management

Product management functionality can improve safety & pharmacovigilance solution by recording and managing details regarding products and dosage regimens while building associations for data accuracy.

Event Analysis

Events analysis functionality helps in creating or reviewing narrative description of cases along with other notes and data for all system events with support for regulatory report information input.

Event Analysis

Events analysis functionality helps in creating or reviewing narrative description of cases along with other notes and data for all system events with support for regulatory report information input.

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