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.