News & Events

  18/01/12

Max Application, in collaboration with Phast Consulting, will attend Assogenerici (italian association of generic drug manufacturers) conference about changing in pharmacovigilance regulation. The meeting is intended to give support to all the companies that have to deal with pharmacovigilance and all the problems, also in term of costs, connected to the new requirements. This meeting will also check associates' willingness to create a joint platform with the purpose of reducing costs and work efforts issued by the new regulation.

Pharmacovigilance - A joint platform for associated companies

Wednesday January the 18th, 10.00 am

UNA Hotel

Via A. de Tocqueville 7/d, Milan

   15/11/2010

SafetyDrugs is now available in Rechargeable Version!

This offer is dedicated to those companies who have to deal with a few adverse events per year.

   25/10/2010

  DIA - Drug Information Association 23 Euromeeting 

  Geneva 28-30 March 2011 

  Visit us at booth  1381.

  We will present you SafetyDrugs.

 26/07/2010

  Max Application announces the new version of SafetyDrugs, available since October 2010.

  Here below you can find the main changes brought to SafetyDrugs version 5.2.6:
 

• New data entry engine to insert data coming from National Pharmacovigilance System (PDF format) directly to the internal database.
• Every case can be automatically or manually acquired by file system and converted, processed and validated. At the end of this process it is saved in the SafetyDrugs database. The system also manages follow-ups.
• SafetyDrugs has been improved with new important informations for Pharmacovigilance System even if they're not required by Eudravigilance (ospitalization, regulatory agencies' comments).
• It is possible to automatically generate the narrative for every case. SafetyDrugs creates its own narrative based on an internal template, using information of the case.
• The system allows to input additional documents (text files, image files... ) and relate them to the case.
   
• For every sender it's possible to manage a list of recipients.
• During the export process SafetyDrugs can create at the same time XML files for every recipient in the list (or just for some of them).

DIA - Drug Information Association

Monaco  8-10  March 2010 

Visit us at booth  206.

We will present you SafetyDrugs.