11 & 12 July 2007 GCP Clinical Studies offices, Rosh Ha'Ayin, Israel EFFECTIVE CLINICAL TRIALS: DESIGN, STATISTICS AND REPORTING Why waste time and money? Running a good clinical trial requires correct planning. Study design, sample-size determination, protocol write-up, statistical analysis, and results reporting are the key elements of an effective clinical trial. We can help you with your clinical trial!

Take Control of Your Clinical Trial Planning!

A 2-day course that offers practical insights on: different study designs and when each is relevant; how to write an effective study protocol; what sample size is necessary; how to select the statistical tests and how to report it all with compliance to regulatory standards and guidelines.

The course provides an understanding of the key concepts and biostatistical issues of clinical trial planning, with an emphasis on practical implications and realistic examples.

It addresses the needs of researchers and research coordinators in both industry and academic medical centers, whether they are new to clinical trials or experienced clinical research professionals.

The course Speakers:

• Diklah Geva, MSc, heads IntegriStat, a biostatistics consulting office.
• Zmira Silman , MA, Biostatistician, consultant to bio-tech companies.
• Tse'ela Schwartz, BSc, biostatistics & medical device Clinical Research Manager , GCP Clinical Studies Ltd.

The Lectures in the course are in Hebrew (Written material in English).

The registration fee includes all course materials, scheduled meals and refreshments.

Enrollment is limited, so register today!

Registration form is attached.
For further details, please contact:
Orna Langerman
GCP Clinical Studies Ltd.
Phone: 03-900-2022
Cellular Phone: 054-4770542

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