management clinical studies, pharmaceutical Data Management, Digital Pen, HP Digital Pen, gathering clinical data, Safety.DB, pharmacovigilance, Adverse Events management, InfoTrials, clinical studies publishing, validation, software web based, clinical trial management, pharmaceutical companies
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e-crf services & systems validation case studies contacts

e-crf, information services and systems for the pharmaceutical world

SERVICES & SYSTEMS

CTDMS management for clinical research activities

Ink.Data collecting data with Digital Pen&Paper

Safety.DB web database adverse events

InfoTrials web publication clinical trials

Validation processes and formal procedures
 

SERVICES & SYSTEMS

The services offered by GM in the line E-CRF include various solutions to the wide-ranging needs of pharmaceutical companies for information technology support.
The experience and know-how acquired by GM over the years alongside the most important international situations have lead to the "Pharma Package", both diversified and easily personalized in relation to the ever new requests of the market.

CTDMS
A technological platform, accessible via web, studied expressly for the management of clinical and/or epidemiologic research studies. CTDMS services include the advanced functionality of Data Management structured in modules, which can also be acquired individually.
 
INKDATA
A service that uses the innovative Digital Pen&Paper technology to offer new methods for the collection and management of clinical data: the data written by hand on the paper CRF by the Investigator is automatically transmitted via internet and made available to the users in various digital formats.
 
 
SAFETY.DB
The application for complying with the implementation of pharmacovigilance: an instrument of advanced web based management of Adverse Events with a modular structure that allows to easily adjust future regulatory standards.
  
INFOTRIALS
The service of GM Pharma for the vital publication of clinical studies on the web, according to the recent guidelines indicated by the most important international pharmaceutical associations.
  
VALIDATION
A process that becomes an integral part of the development of a system: GM offers its support defining also the formal procedures up to the construction of a Validation Master Plan necessary for validating registration clinical studies. All of the validation protocols are provided in English.

Each system realized is a world unto itself, a unique reality: because the needs of our Clients are unique and unrepeatable.
It is for this reason that every project becomes a challenge: GM is specialized in developing projects on order, whether integrating advanced technology into preexisting systems or planning complete applications in support of the Client’s activity.
Contact us: we will be pleased to work together for the answer to your needs.

ISO 9001:2008 e ISO 27001:2005 E- CRF complies with GM Servizi srl Quality Management System certified for ISO 9001:2008
and for Information Security Management System certified ISO 27001:2005
ISO 9001:2008 e ISO 27001:2005