Come and find the answers with 4 parallel conference tracks on Regulatory Affairs in Emerging Markets, IDMP Compliance, Global eSubmissions and Biosimilars

Regulatory Affairs in Emerging Markets

Understand the requirements. Successfully register your products. Ensure regulatory compliance: Russia, CIS countries, Turkey, the Middle East, Africa, LATAM and APAC.

IDMP Compliance

Are you IDMP ready? Let us help with your preparation: 18 regulatory agency and industry experts, case studies and interactive sessions to show you the pathway to compliance.

Global eSubmissions Focus Day

Look no further to ensure a robust global submission strategy. Updates from Europe and latest eCTD progress in the GCC, Jordan and China to ensure you meet latest requirements.

Biosimilars

Market access, Business and Commercial Strategies. Regulatory and CMC landscape. Clinical and non-clinical developments: Regulatory agency advice, industry experts and in-depth discussion.

25% discount for EXTEDO customers

To receive an exclusive 25% conference discount*, use the VIP code: CQ5267EDO when registering.

More details and registration

https://lifesciences.knect365.com/global-pharma-regulatory-affairs/

*Discount Ts and Cs:

1) 25% discount not applicable to supplier/vendor companies. KNect365 Life Sciences will verify whether you are a supplier/vendor when your registration is processed. 

2) Discount not to be used in conjunction with any other discount.