Other services used

Medical writing

Pharmnet medical writers have experience in the preparation of 15 study protocols in various therapeutics areas (neurology and psychiatry, cardiology, vaccines). In addition to the study protocols, there are dozens of CRFs, Informed Consents and other documents compliant with the ICH-GCP and local legislation created for our clients.

Pharmnet Medical Writers completed over 20 Clinical Study Reports (trials phases II-IV).

Our Medical writers are also authors of presentations and papers for medical journals.

Auditing

Pharmnet auditors performed site, vendor, office and system audits in the following countries: Czech Republic, Russia, Ukraine, Poland, Slovakia, Estonia, Latvia, Georgia, Bulgaria and Romania.

Trainings / Meeting organization

Senior Pharmnet staff has provided dozens of lectures and training courses to the investigators and clients employees, either as a part of the scope of the clinical trial management or upon request of our clients. These trainings were focused on GCP and local legislative requirement, general research methodology and applied statistics.

Data Management and MedDRA coding

Recently, Pharmnet offers Data Management services in cooperation with our partners.

Our management capabilities are based on long term experience with the Data Management services from the past when these tasks were covered with internal resources. We have completed more than 50 studies including data management and statistical evaluations.

We have over 10 years of experience with MedDRA coding (English, Czech language). Coding is done by our internal physicians.  

NIS / Pharmacoeconomic surveys

We have worked on more than 10 non-interventional projects. We were involved in 4 pharmacoeconomic studies (e.g. cost effectiveness of psychiatriatric treatments, or a market potential of a biological graft in burns). Work on these studies comprised of preparing protocol, clinical study report and publications.

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