Global Pharmacovigilance

There is an array of documents which have to be generated and updated periodically (safety reports). We have extensive experience in preparing and maintaining high quality documents to ensure compliance with requirements.

These include safety reports as:

  • Mandatory RMPs for all products
  • PSURs required periodically and post-authorisation
  • DSURs that need to be provided on an annual basis

We can review your current documents to ensure continuous compliance or prepare new ones ready for submission.

We have access to a wide range of databases and extensive hands-on experience, allowing us to produce the most accurate literature results in the literature searches conducted to support these activities.

Business Cases

  • Case Study detail

    Local Pharmacovigilance Management

    Global Pharma Company, United States
  • Case Study detail

    Full outsourced EU Pharmacovigilance system

    Leading Generic company, North America

Contact Us

If you want to dicuss how you can be safe in our hands, please contact us for a consultation.

Telephone: +353 125 44033
Email: marketing@arriello.com

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