CPhI Korea 2018 Conference Pre-Registration
Deadline : 22nd August, 2018
Choose your Preferred Sessions
See conference timetable
Please check the number of session that you would like to register.
One - USD 70.00
Two - USD 126.00
Three - USD 178.50
Four - USD 238.00
Five - USD 297.50
Six - USD 336.00
Seven(ALL) - USD 367.50
Please check the sessions that you would like to register.
Please choose the same number of sessions you have been chosen above.
Session 1. Experience of GMP Inspection at PMDA and Future Perspective of GMP in Japan (PMDA, Japan)
Session 2. Claims for Foods in the European Union: Key Regulatory Features / Claims for Foods in the EU: Regulatory Checklist (EAS Strategies, EU)
Session 4. The US Complex Generic Products & Biosimilar Product Regualtory Approval Process / US FDA Pre-approval and Routine cGMP Inspections for Complex Generic and Biosimialr Products ((Insight, Advice & Solutions, USA, ex-FDA CDER regulator)
Session 5. Recent Trends in the EU Market / Implementation of ICH Q3D (elemental impurities) for APIs - Practical examples (APIC, EU)
Session 6. The Biologics Drug Development in China - CMC and Quality Challenges 1 & 2 (Suzhou AAbioQ, China)
Session 7. Nutrition and Health Food Claim Regulations in China & What They Mean to Consumers / Trends Impacting the Health Food Market in China (China Skinny, China)
Session 8(Language-Korean ONLY). Changes in ICH E6 GCP(R2) and Issues Concerning Safety Evaluation and Reporting of Clinical Trials / Current Trend in Pharmaceutical GMP Policy (MEDI-INSIGHT Corp. / MFDS, Korea)
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