AB Cube

The Safety Software Company

We design safety software and we are doing It well.

During the last 10 years AB Cube has designed pharmacovigilance, medical device vigilance and cosmetovigilance software.

But AB Cube provides much more than safety software : A close relationship with its customers, a full service (including updates, support, validation, …) and tools dedicated to compliance and security (Ticketing, Validation software, eLearning LMS system, … ). Let’s discover our solutions.

 

Have a Closer Look

SafetyEasy PV Human

Your Human Pharmacovigilance Software database

SafetyEasy PV VET

Your Veterinary Pharmacovigilance Software database

SafetyEasy Device

Your Medical Device Vigilance Software database

CosmEthics

Your Cosmetic Safety Software database

SafetyEasy NUTRI

Your NutriVigilance Software database

SafetyEasy MI

Your Medical Information Management Software database

Few numbers ….

# of Database Installed worldwide

# of users

# of cases handled


Testimonials

After having been using SafetyEasy PV for 8 years, Air Liquide Santé International has decided to use SafetyEasy Device too, since we have been very satisfied of the first AB Cube’s PV software database.

Air Liquide Santé International has to deal at an international level with Pharmacovigilance and Medical Device Vigilance of clinical trials and we need to have a secured, reliable, and user friendly software to be compliant with both safety requirements.

More than just a software vendor, AB Cube has been for 8 years an important partner in our regulatory compliance.

Hubert PONCELET

Global Head, Pharmacovigilance - EU QPPV - Healthcare Global Operations, Air Liquide Santé International

Laboratoires SMB are active in the development, manufacturing and marketing of human pharmaceutical products.
All these steps in the life-cycle of a pharmaceutical product involve specific pharmacovigilance activities that require appropriate tools, including software.
In that context, for about ten years, we have been using two AB Cube’s tools, SafetyEasy PV Human and SafetyEasy MI who have found their places in our pharmacovigilance system. SafetyEasy PV Human for the management of clinical and post marketing pharmacovigilance cases and SafetyEasy MI for the management of medical information related to our products launched on the market.

For both software, among others, we appreciate on the one hand, their friendly use and customization capability, and secondly, their ability to evolve and adapt to the current guidelines. When you add the support offered by AB Cube and the responsiveness of its team, we can claim to be satisfied with the services of AB Cube. Therefore, we recommend enthusiastically AB Cube’s software to companies with pharmacovigilance requirements.

 

Dr Lucas Fotsing

EU QPPV & API Director, Laboratoires SMB SA

AB Cube Solutions provide you with Integrated Pharmacovigilance Software but also

Compliance

Validation

  • GAMP 5 validation
  • On-line valdation dossier available
  • Validation dossier updated
  • Minimum validation effort

Full services

  • Transparency (Access to online Document Management system)
  • eLearning
  • 24 / 7 hotline
  • Validation software
  • Ticketing software

Secured & Reliable

  • HIPAA compliant
  • SSL web access
  • BackUp & Restore
  • 99,99 % SLA guaranteed
  • 21 CFR part 11 Full Audit Trail
  • ISO 27001 data center (Tiers III plus)

Fast & User Friendly

  • Full web (pure HTML)
  • All web browser compatibility
  • Customization available
  • Easy and fast Data Entry
  • Fully customizable WorkFlow

Fair pricing

  • No hidden costs
  • Clear and adaptative offer (From Basic to Professional)
  • Unlimited number of users

SaaS & On-Premise

  • Hosted solutions
  • On-Premise solution
  • Great experience in data migration

Scalable & Flexible

  • Full Query module integrate
  • Totally customizable by end users
  • Fully customizable Work Flow

Latest News

Green light given for new EudraVigilance system : 22th November 2017

Green light given for new EudraVigilance system for collection and monitoring of suspected adverse reactions In summary, the simplified electronic reporting of suspected adverse reactions related to medicines by national Competent Authorities and marketing...

ICH E2B (R3) specifications have been updated

New E2B (R3) package is vailable here : http://estri.ich.org/e2br3/index.htm

New EMA Gateway Validation process in June 2017

The new process for validating your ICSR Gateway will be available in June 2017

New DIA Training Program has been launched

As learning is a continuous process, we want to let you know that the 2017 dates for EudraVigilance Courses are now open for registration – new dates are available below! Help us spread the word and let your colleagues know about these excellent opportunities...

7th Annual Pharmacovigilance & Risk Management Strategies : 25th -27th january 2017

Contact us ! It’s a unique occasion to meet at this conference in Amsterdam https://fleming.events/events/pharma/pharmacovigilance-risk-strategies-forum

23th – 25th January 2016 : DIA Pharmacovigilance in Washington D.C.

http://www.diaglobal.org/en/conference-listing/meetings/2017/01/dia-pharmacovigilance-and-risk-management-strategies-2017 Come and visit us !

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