- e-Learning -
Webcode 22122497
Lidia Cánovas
ASPHALION S.L., Barcelona, SPAIN
General Manager
anytime
anytime
online
online
Event - 390,- € plus tax
The fee for a single account that is valid for 90 days is €390 (excluding German VAT). You can access the modules as often as you want during this time. You will be awarded a certificate of completion at the end.
Our general terms and conditions (dated 1 November 2021) apply and are available upon request. We can send them to you anytime or you can find them on the internet at www.forum-institut.com/t&c. Please refer to the section 'Special terms and conditions for online offers'.
Event - 390,- € plus tax
The fee for a single account that is valid for 90 days is €390 (excluding German VAT). You can access the modules as often as you want during this time. You will be awarded a certificate of completion at the end.
Our general terms and conditions (dated 1 November 2021) apply and are available upon request. We can send them to you anytime or you can find them on the internet at www.forum-institut.com/t&c. Please refer to the section 'Special terms and conditions for online offers'.
Dr. Birgit Wessels
Conference Manager
+49 6221 500-652
b.wessels@forum-institut.de
This e-Learning programme will familiarise you with the data requirements in CTD Module 3.
Module 3 is an essential part of the CTD. It presents data on the quality of the drug substance and drug product. But what data is required? How should Module 3 be structured? These are the topics of our e-learning programme.
In this e-Learning you will:
This e-Learning programme addresses the needs of those working in the pharmaceutical industry. It will particularly benefit those needing a good knowledge of the structure and content of CTD Module 3.
Here you can get a brief insight into the e-Learning CTD Module 3.
The 'CTD Module 3' e-learning programme comprises four didactic modules that include videos in which expert Lidia Cánovas shares her expertise with you. You can also download and print the corresponding presentation documents. Each module also includes additional documents (links, guideline texts, etc.). The e-learning ends with an online test, which helps you practise and apply your newly gained knowledge. Once you have completed the four modules and passed the test, you will be awarded a certificate, which you can print out directly. The e-learning programme should be completed within three months.
Modules
Hours of learning content
e-Learning course with six modules on how to initiate and manage collaborations with patients and patient organisations ...
This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of var...
This e-learning will familiarise you with the regulatory affairs principles outside the ICH region and show you how to c...
Do you need know how regarding CTD/eCTD & CMC? Then this e-learning programme is the fast track to becoming knowledgeabl...
This e-learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketi...
Are you interested in our international continuous education programme? We provide a variety of specialised courses.
Details
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