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Certificate course in electronic submission standards from SGS – understand all aspects of electronic drug registration, including regulatory and electronic data management for clinical research.

Clinical trials often involve tedious, manual processes for collecting, aggregating and rationalising information from data sources. To make the process faster and more efficient, food and drug administration departments are moving towards electronic management and review of approval data. This course will help you to understand the electronic submission process which is considered to be the future of clinical trials monitoring.

Why choose the certificate course in electronic submission standards from SGS?

This course can help you:

  • Understand the electronic drug registration process
  • Streamline processes, aptly respond to current statuses and manage your clinical trials more effectively
  • Learn about the main issues of conducting clinical studies
  • Discover the requirements for training and regulatory compliance for working in an electronic environment

The trusted certificate course in electronic submission standards from India’s leading training provider

As a leading course provider in India, we provide unrivalled experience and expertise in training for all aspects of clinical trials monitoring. Plus, as a world leader in certification, verification, inspection and testing we offer you in-depth knowledge gained from conducting clinical trials monitoring for leading pharmaceuticals across the globe. In addition, we keep up-to-date on the very latest principles and issues in clinical research and data management, so you can rest assured that you will be knowledgable of the latest changes.

To find out more about certificate in electronic submission standards, contact us today.