Safety in Clinical Trials: Can we help you?

July 18, 2023

The safety management of a clinical trial (CT) is one of the most relevant activities during its execution, starting from the very beginning with its planning, and requires the involvement of professionals with extensive experience and a continous specific training.

In addition to this, in Europe safety management is a regulated and mandatory activity, since it is necessary to guarantee the safety of patients and ensure the robustness and integrity of the data obtained about the safety of the investigational product. Constant monitoring of the benefit/risk profile of the product under development should be carried out through continuous analysis of each adverse event and the preparation of safety reports.

Leave the safety of your trial in the hands of Asphalion! At Asphalion, we can help you in the comprehensive management of security activities and in the global management of any type of CT you want to carry out.

Have a look at the infographic we have prepared: ASPHALION Pharmacovigilance in Clinical Trials 

If you are interested in getting more details about our Clinical Trials services, do not hesitate to contact us: [email protected]

You can also book a free 30-minute meeting: SCHEDULE A FREE MEETING HERE

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Many key takeaways and highlights from the DIA RAPs Regulatory Policy Forum!! Capitalizing on the success of their joint collaboration this past January for 2024 Combination Products in the EU, DIA and the Regulatory Affairs Professionals Society (RAPS) are coming together once again to produce the 2024 Regulatory Policy Forum.
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