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”.

Days

Hours

Minutes

Seconds

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.

Upcoming Events

Join Our Seminar

Our Speakers

Key Themes

Who Should Attend?​

Who Should Attend?