We manage post-marketing Pharmacovigilance activities for pharmaceutical companies that need complete and timely outsourced services to implement and maintain a pharmacovigilance system in accordance with the current legislation.

EU Regulations require each MAH to establish and maintain a PV system.
Our outsourcing proposals are highly customizable to Clients’ needs: from a global management of PV System to spot services.

  • QPPV Local QPPV

  • PSMF writing and/or revision

  • Literature screening

  • Signal Management

  • Third party management

  • PV Training



ACCELERATE YOUR CLINICAL DEVELOPMENT PROGRAM WITH CROlife Services include project management through to clinical trial monitoring, management and patient recruitment. CROlife has established relationships with trial sites, key [...]