Although ACTide is used by all types of customers and industries -whether they are Pharmaceutical or Medical Device companies, research institutions, non-profit organizations, or hospitals-, it is CROs that are historically the designated target audience for our platform. ACTide is fully featured with the Sponsors’ most requested functionalities; it also comes with an encompassed flexibility in terms of configuration, usage, and pricing that make it the perfect solution for CROs. ACTide's clinical services are the perfect companion to your projects based on our platform and are declined with the same level of flexibility. Our data management team is engaged with your project from the very beginning until the study decommissioning to support your team throughout the study lifecycle.
Industries
Pharma
ACTide is the flexible and affordable solution for the pharmaceutical industry. Optional modules, along with a flexible service model, allow you to tailor the solution to the real needs of your projects/studies, thereby lowering the TCO per study by minimizing system complexity.
Medical Devices
EDC medical device clinical trials software must meet a variety of requirements related to connectivity, security, privacy, API integration, and specific interfaces to hardware. Medical device companies must be forward-looking and provide their data to post-market safety surveillance, compliant with regulatory authorities’ expectations.
Animal Health
ACTide complies with VICH GL9 (CGP) and is the perfect solution for your clinical animal health trials. Specific features have been created and configured to meet the particular needs of Data Capture in Animal Health scenarios.
Non Profit
The flexible service model and the extreme granularity in the configuration of the CRF allow a very favorable price level, even for low budget or non-profit projects. Added to this is the ability to further split the TCO by outsourcing part of the study's CRF design process.
Services
eCRF Self-Configuration
ACTide flexible workflow gives your project-managers unlimited freedom to design and configure your eCRF. It helps create validation rules, manage users and sites. You can define and set normal ranges for laboratory data, preview your draft at any time to have a working environment to show to your customers.
Intermediate Tactical Choices
Rely on the ACTide® Team for complex or critical tasks and use your staff for the rest. You decide the balance between internal and external effort to match your budget requirements and your production pipeline.
Full Service by Nubilaria
Fully delegate to the experienced ACTide Team staff the task of building and validating your eCRF and see the magic happen. Focus your team on your core duties and tasks and let the ACTide Team to complete your eCRF fully compliant with project requirements.
Cases
According to the Epidemiology National Centre, between 1% and 5% of the population over 65 and 30% of the over 80 suffer from dementia. These figures mean over 20.000 cases within the city of Milan only. Alzheimer is responsible for over 50% of all such cases. It has been estimated that in Europe by 2030 there will be over 65 million people suffering from Alzheimer.
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News & events
All / Events / News
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29-30/11/2023
Nordic Life Science Days (NDL)
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Coming November 2023
European Trial Master File Summit
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24-26/10/2023
CPhI
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20-24/10/2023
ESMO
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10-12/10/2023
Festival of Biologics
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27-29/09/2023
ExpoPharm
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10-11/05/2023
Global Clinical Trials Connect
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24-26/05/2023
XXX Congresso Nazionale GIQAR
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09-11/05/2023
Vitafoods Europe
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03-04/05/2023
Outsourcing in Clinical Trials Europe
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25-27/04/2023
DMEA Connecting Digital Health
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24-25/04/2023
Swiss Biotech Day
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20-22/03/2023
BIO Europe Spring
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12-14/03/2023
ACDM Conference
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06-08/03/2023
Animal Health, Nutrition and Technology Innovation Europe
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INFORMATION REQUEST
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