Upcoming Events
POWERTALK
7 June 2024
- Time : 13.00 – 15.00 WIB
- Offline Venue: Room 208
- Online venue: Zoom (Link will be given one day prior to the Event)
- Participants will get e-certificates
COMPETITION
3 July 2024 (Registration closed)
- Preliminary Round (1 May – 3 Aug 2024)
- Semifinal Round (10 – 25 Aug 2024)
- Final Round (31 Aug – 8 Sep 2024)
- Win Rp 12,5 Million for first place
- Claim up to Rp 1,5 Billion scholarships
SUMMER PROGRAM
8-11 July 2024
- Eligible for Elementary, Junior, and Senior High School Students
- Venue: i3L Campus and Inagro Park
- Claim discount 20% for group registration
Join Our Seminar
The pharmaceutical industry is witnessing a transformative shift towards continuous manufacturing, fueled by advancements in Process Analytical Technology (PAT) and Real-Time Release Testing (RTRT). This seminar aims to explore the integration of these innovative solutions and their profound impact on enhancing efficiency, flexibility, and quality control in drug production.
We invite you to join this year’s seminar, entitled “Continues Manufacturing, PAT, and RTRT: Envisioning the Future of Pharmaceutical Industry”.
Our Speakers
Dr. Ria Christine Siagian, S.Si., Apt., MSc
- Position: Head of Drug Registration Unit, Directorate of Drug Registration, BPOM (Indonesian FDA)
- Topic: Regulatory Aspect of Real-Time Release Testing, Process Analytical Technology, and Continuous Manufacturing
Noviani Rustanto
- Position: Head of Marketing, PT. Virtus Analitika Mitratama (sole distributor of MicroNIR)
- Topic: Application of Process Analytical Technology in Pharmaceutical Industry
Bart Stynen, MSc
- Position : Area sales manager
- Topic : Application of Continuous Process Manufacturing in Pharmaceutical Industry
Ardhian Tirta Kusumawan
- Position: Quality Assurance Manager, PT Kalbe Farma Tbk
- Topic: Application of Real Time Release Testing in Pharmaceutical Industry
Key Themes
- Understanding the principles and benefits of continuous manufacturing
- Exploring the role of PAT and RTRT in enhancing quality control and process monitoring
- Regulatory considerations and compliance in adopting continuous manufacturing practices
- Real-world applications and case studies demonstrating successful implementation
- Strategies for overcoming challenges and maximizing the potential of continuous manufacturing
Who Should Attend?
- Professionals from pharmaceutical manufacturing companies
- Regulatory affairs professionals
- Quality control and assurance personnel
- Researchers and academics in pharmaceutical sciences
- Consultants and industry experts interested in advancements in pharmaceutical manufacturing
Join us for an insightful exploration of the future of pharmaceutical manufacturing! Let’s pave the way towards excellence in drug production through continuous innovation.
