Case Study

Case study is to maintain a prospective representative database of the treated population during normal clinical practice, aimed to provide data on clinical safety, and closely monitor the usage of the product and monitor the use of the product in clinical practice. Collection of case report form(CRF) via hybrid solution.

  • Periodic safety update reports
  • clinical trials on various disorders
  • All AE/SAE handling and databasing
  • protocol and CRF design
  • Ongoing monitoring of events

Related Conference of Case Study

September 20-21, 2017

10th Pharmacovigilance Congress

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(10 Plenary Forums - 1Event)

6th International Conference and Exhibition on GMP, GCP & Quality Control

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12th World Pharma Congress

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11th World Drug Delivery Summit

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10th International Conference and Exhibition on Biologics and Biosimilars

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4th European Biopharma Congress

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9th Asian Biologics and Biosimilars Congress

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Case Study Conference Speakers

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