Privacy Policy - Regulation, Quality and Compliance in ADC Manufacturing
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Privacy Policy

This course provides a practical understanding of data technologies used in clinical trials and is intended to provide attendees with the latest regulations, guidelines and requirements for using electronic data in clinical trials. With the recent widening of the guidelines and regulations to encompass electronic data, it is essential that all persons involved in any aspects of clinical trial data understand the principles and intent of the regulations. Companies must ensure that the QMS processes used in the management of clinical trials fully cover all areas of the regulations in relation to the management and integrity of clinical trial data.

We are committed to protecting and respecting your privacy. This policy together with our Terms & Conditions and any other contractual documents which sets out the basis on which any personal data we collect from you, or that you provide to us, will be processed by us. Please read the following carefully to understand our views and practices regarding your personal data and how we will treat it. By entering into a Sales Agreement with IGR Events you are accepting and consenting to the practices described in this policy. The purpose of processing personal data is to use them to fulfill a consumer contract that the seller concludes with the buyer by creating an order in this online platform.

Personal data will not be given to third parties. For the purpose of facilitating networking, event participants may also have the access to the following information about other participants attending the same event: name, surname, email, job title, company, country.

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A comprehensive training schedule containing all the crucial information will be delivered to your email inbox.