One of Pharmalink Consulting's experienced consultants accessed the documentation via secure portal and began work immediately.
The consultant pieced together the product history from the original submission and subsequent maintenance activities (variations/supplements and annual reports) and prepared a QOS ahead of schedule.
The consultant was also able to add value by preparing a risk analysis alongside the required output, thus ensuring that the client was aware of potential issues once the filing was undertaken.
The work took the consultant 35 hours to complete and was delivered to the client less than one week after the request for the work was received by Pharmalink Consulting.
