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You now have access to the latest updates, events and resources.
Event Registration successful
You now have sucesfully register for the event and you can also access the latest updates, events and resources.
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Account activated – pending validation.
Your account has been activated successfully, but we still need to validate you as a healthcare professional. We’ll send you an email with the result of the validation process in the next [five] days.
In the meantime, you can enjoy access to all the latest news, events and resources on our website
Event registration completed - pending validation.
Your account has been activated successfully, but we still need to validate you as a healthcare professional. We'll send you and email with the result of the validation process in the next [five] days.
In the meantime, you can enjoy access to all the latest news, events and resources on our website
In case you would like to receive sms-reminders for the event you have registered, please update your communication preferences here.
Account activated - pending validation.
Your account has been activated successfully, but we still need to validate you as a healthcare professional. We’ll send you an email with the result of the validation process in the next [five] days.
In the meantime, you can enjoy the public content on our website
Event Account activated - pending validation.
Your account has been activated successfully, but we still need to validate you as a healthcare professional. We’ll send you an email with the result of the validation process in the next [five] days.
In the meantime, you can enjoy the public content on our website
In case you would like to receive sms-reminders for the event you have registered, please update your communication preferences here.
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To report an adverse event or product complaint, please contact GlaxoSmithKline on 0800 808 500 or complete the form below.
Thank you for taking the time to report an adverse event or product complaint. GSK routinely monitors the quality and safety of all our medicines. This includes review of safety data from clinical studies, and collection of adverse event reports for marketed products.
This information contributes to the continuing quality and safety surveillance of our products.
