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Clinical Trial Project Management

PharSafer® can help in the management of Clinical trials.  We can ensure that sites are properly managed and supported by Clinical Trial Monitors and that the rigid ICH E6 Good Clinical Practice Standards are being met whatever the size of location of the clinical trial.

The monitors can help in set up, maintenance and site closure post clinical trial conclusion too.

Additionally, our services extend beyond the safety processing aspects of Clinical Trials to include; Safety Investigator Brochure writing, help with CRF design, Medical monitoring, Investigator training,  SOP writing and GCP auditing.

PharSafer® Tweets

The @EU_Commission and @EMA_News have released their latest communication, regarding a one year delay to the MDR 2… t.co/AvgeN17Qo8

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UPDATE: @MedDRAMSSO has released its guidance for the correct usage of new coronavirus specific terms, when reporti… t.co/k3TwufyaY6

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The @EU_Commission and @EMA_News have released guidance for the safe management of clinical trials during the COVID… t.co/AMPtGLvRKu

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