- Online training -
Webcode 22032450
Dr. Christina Juli
Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss
Head of Technical Regulatory Affairs
Pooja Maingi
PharmaLex India Pvt. Ltd., INDIA
Associate Director, Head of Regulatory Affairs India
Galina Senchukova, PhD
CSL Behring Biotherapies, Moscow, RUSSIA
Head of Product Market Authorization and Quality Assurance, PhD in Pharmaceutical Chemistry. 20 years in regulatory area in total: for 6 years - Tutor of Pharmaceutical Chemistry at Pharmaceutical State University (Pyatigorsk, Russia), 9 years of experience in Drug Product development for Russian manufacturers and 6 years - in local batch release quality control; 11 years in Big Pharma RA departments.
Jack Wong
Founder of Asia Regulatory Professsionals Association, Singapore
Over 25 years of Regulatory, Quality, Clinical Trial and Pharmacovigilance experience in Asia with good knowledge in the field of Nutritional, Pharmaceuticals, Medical Devices, Consumer Healthcare and Biological products. Externally, playing a leading role among all the Regional Regulatory professionals in AHWP (Asian Harmonization Working Party). Being the founder of ARPA (Asia Regulatory Professionals Associations) since 2010 with over 4800 members. Adjunct Lectureship & Visiting Professorship with Nanyang Technological University (Singapore), Tohoku University (Japan), Beijing University (China), Chinese University of Hong Kong (Hong Kong), University of Hong Kong (Hong Kong), Taipei Technical University (Taiwan), University of Sydney (Australia), Dongguk University (Korea)
anytime
anytime
10 March, 17 March, 24 March, 31 Mar...
10 March, 17 March, 24 March, 31 March
live webcast from 10:00 am - 12:15 pm
You may dial in 30 minutes before the training starts.
online
online
Event - 1.190,- € plus tax
The fee includes a documentation for download and a certificate.
SPECIAL OFFER
Data requirements in the EU
, online
Simply register for the seminar and receive a €50 discount on the e-learning programme (€340 + local VAT rather than €390 € + local VAT) if you book it simultaneously.
340,00 €
Event - 1.190,- € plus tax
The fee includes a documentation for download and a certificate.
SPECIAL OFFER
Data requirements in the EU
, online
Simply register for the seminar and receive a €50 discount on the e-learning programme (€340 + local VAT rather than €390 € + local VAT) if you book it simultaneously.
340,00 €
Dr. Birgit Wessels
Konferenzmanagerin Healthcare
+49 6221 500-652
b.wessels@forum-institut.de
Four live webcasts à 2 hours every week in March 2022: CMC requirements in China, India, Japan, South Korea and Russia/EAEU. Meet our four experts to get an update on the current requirements in the different regions and discuss your individual issues with them. You are interested in one webcast only or a group account? Contact us!
During this webcast series you will learn about the specific CMC requirements in China, India, Japan/South Korea and Russia/EAEU.
Four (local) experts will share valuable information regarding
This series will be of benefit to all those working in the pharmaceutical industry, particularly CMC and regulatory affairs managers, who are dealing with dossier compilation (quality data/module 3) for the regions China, India, Japan/South Korea and Russia/EAEU.
The webcast series will cover small molecules and biologics too.
10:00 Welcome, introduction round, expectations
10:10
Jack Wong
12:00 Summary and outstandig questions
12:15 End of webcast
10:00 Welcome, introduction round, expectations
10:10
Pooja Maingi
12:00 Summary and outstandig questions
12:15 End of webcast
10:00 Welcome, introduction round, expectations
10:10
Dr Christina Juli
12:00 Summary and outstandig questions
12:15 End of webcast
10:00 Welcome, introduction round, expectations
10:10
Dr Galina Senchukova
12:00 Summary and outstandig questions
12:15 End of webcast series
Our online training courses are live and interactive. They are held and controlled directly by our speaker. You may take part in the seminar from anywhere using your end device. You will see the presentation and listen to our speaker's lecture using Internet telephony (VoIP) or even a normal telephone connection. And you can also ask questions live.
Overall score of all evaluations in 2021
Five stars on Trustpilot = Excellent
Our biotech experts will provide you with the latest information on issues related to development, quality and regulator...
Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...
Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...
Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...
Our biotech experts will provide you with the latest information on issues related to development, quality and regulator...
