2020 PDA Asia Pacific Aseptic Processing of Biopharmaceuticals

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English

한국어

ไทย

中文

The Virtual Conference will give an update on the manufacturing of sterile products and patient-friendly application systems. The goal is to present the latest on new technologies in fill-finish operations with the upcoming GMP regulations (Annex 1) in mind. The conference will also include insights into market and technology trends for more patient-friendly injection systems.

Presentation topics will be divided into two parts:

Manufacturing:

Barrier Systems
Filling Lines & Filling Systems
Aseptic Process Simulation
Smoke Studies
Container Integrity Testing
Visual Inspection

Container Closure Components and Devices:

Container Closure Components: Glass, Elstomers, etc.
Elastomer Processing
Elastomers for Cryogenic Storage, Deep Freeze Sealability
Market Trends in Patient-Friendly Injection Systems
Devices: Pens, Autoinjectors, and Wearables

*Please note that the Virtual Conference will run according to Korea Standard Time, GMT+9

**Simultaneous translations in Korean will also be made available

Agenda

Monday, October 12, 2020 11:00^AM to 6:15^PM: 11:00^AM - 11:10^AM
Welcome & Introduction | Korea Standard Time, GMT +9; 11:10^AM - 12:40^PM
Keynote 1: Aseptic Manufacturing in Times of Covid-19: Supply Chain, People, Management; 12:40^PM - 1:10^PM
Keynote 2: Regulatory; 1:10^PM - 1:25^PM
Sponsor Demonstration: Charles River Laboratories Korea; 1:25^PM - 2:00^PM
Break

Tuesday, October 13, 2020 11:00^AM to 6:45^PM: 11:00^AM - 2:00^PM
Manufacturing: Container Integrity | KOREA STANDARD TIME, GMT+9; 2:00^PM - 2:15^PM
Sponsor Demonstration: MERCK; 2:15^PM - 2:30^PM
Break; 2:30^PM - 4:30^PM
Manufacturing: Filling Specifics; 4:30^PM - 4:45^PM
Break