Master Data Management

Key Features

Key partnerships with leading MDM technology vendors
  • Our deep expertise in the life sciences industry combined with partnerships with leading MDM technology vendors like Reltio, Informatica and Semarchy enables us to offer cutting-edge solutions for enhanced engagement, experiences and transformation in a multitude of life science use cases.
Industry-specific data models for life sciences domain
  • Empowers you with industry-specific and customized data models to give you a significant head start and edge in data integration and mastering efforts, and effectively leverage all your organizational data assets.
Adapters for data acquisition from clinical systems
  • Enables you to augment and consolidate data from across multiple and siloed internal and external sources to ensure a ‘single source of truth’ and to increase cross functional collaboration with a foundation of trusted data.
Better compliance to regulatory requirements
  • Enables better compliance to regulatory compliance requirements such as IDMP, GDPR, HIPAA in terms of clinical data management, site selection, study processes, etc., to enable faster submissions and ensure frictionless approvals.
Adherence to standards and best practices
  • Ensures greater adherence to standards and best practices for match & merge and create golden records.
Implementation accelerators & templates
  • Offers a range of implementation accelerators and templates to enable you to eliminate incessant delays in trials, processes, study startup, site selection, patient recruitment, payments, R&D, time-to-market, etc. and drive overall efficiency, agility and profitability.

Use Cases


Investigator & Site Selection for Clinical Trials 

Leverage MDM-driven solutions to identify, onboard, engage and effectively work with competent investigators and sites for accelerated clinical development.
 


Speedy Patient
Onboarding
 

Leverage MDM-driven solutions to identify and select the most suitable patients for clinical trials and onboard them in a speedy manner to accelerate study startup.

Clinical Data
Integration
 

Leverage MDM-driven solutions to check study feasibility, master clinical data (study, site, investigator, subject, visit etc.) and reference data (region, therapeutic area etc.)
 

Molecule to Market 

This IDMP compliant solution provides a head start and strategic edge in drug discovery, R&D, RWE, manufacturing and marketing authorization by being an authoritative source for medicinal products.

New Drug Commercialization 

Develop a detailed, comprehensive commercialization plan and effectively manage it to effectively engage in cross-functional activities across multiple organizations necessary to successfully execute the launch of new drugs.

Investigator & Site Selection for Clinical Trials 

Leverage MDM-driven solutions to identify, onboard, engage and effectively work with experienced and competent investigators and sites for accelerated clinical development. Eliminate costly delays, errors and other challenges that make clinical trials inefficient and expensive.


Speedy patient onboarding 

Leverage the MDM-driven solutions to identify and select the most suitable patients for clinical trials and onboard them in a speedy manner to accelerate study startup.

Clinical Data Integration 

Leverage MDM-driven solutions to quickly check study feasibility, master clinical study, site, investigator, subject, visit, etc., and referential entities like region, therapeutic area, etc. Integrate patient and operational data for analytics and effective monitoring.

Molecule to Market 

This IDMP-compliant solution is an authoritative source for medicinal products from active ingredients to the packaged products. Leverage this solution to give yourself a head start and a strategic edge in drug discovery, R&D, real world evidence, pharmacovigilance, manufacturing, authorization and others.

New Drug Commercialization 

Develop a detailed, comprehensive commercialization plan and effectively manage it to effectively engage in cross-functional activities across multiple organizations necessary to successfully execute the launch of new drugs.

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