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ICCLMPC · Registering as Listener

International Conference on Clinical Laboratory Medicine, Pharmacy and Chemistry

13 - 14 Nov 2026 Jakarta Raya, Indonesia Standard / Physical Participation
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$120
virtual · $135 in person
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Registration summary

ConferenceICCLMPC
ModeStandard / Physical
ParticipationListener
Registration fee$135.00
Bank charges (5.8%)$7.83
Total payable$142.83
Includes all bank processing charges — the amount above is exactly what will be charged.

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Benefits of Registering as Listener

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Conference Kit / Materials
Access to Keynote Sessions
• Conference Session Tracks •
SDGs
SDG-Aligned Research Themes

ICCLMPC conference tracks support global knowledge exchange, innovation, and sustainable development priorities across diverse disciplines.

SDG 3 - Good Health and Well-being SDG 4 - Quality Education SDG 9 - Industry, Innovation and Infrastructure SDG 12 - Responsible Consumption and Production
01 Advancements in Pharmaceutical Chemistry +
This track focuses on the latest developments in pharmaceutical chemistry, emphasizing innovative methodologies in drug design and synthesis. Participants will explore cutting-edge research that enhances the efficacy and safety of pharmaceutical compounds.
02 Clinical Pharmacy Practices and Innovations +
This session will delve into contemporary practices in clinical pharmacy, highlighting innovative approaches to patient care and medication management. Discussions will include the role of clinical pharmacists in optimizing therapeutic outcomes and improving healthcare delivery.
03 Analytical Techniques in Laboratory Medicine +
This track will cover advanced analytical techniques employed in laboratory medicine, focusing on their application in diagnostics and research. Participants will gain insights into the latest technologies that enhance the accuracy and reliability of laboratory results.
04 Translational Research in Pharmacy +
This session will explore the intersection of basic research and clinical application in pharmacy, emphasizing translational research methodologies. Attendees will discuss strategies for bridging the gap between laboratory discoveries and practical therapeutic solutions.
05 Quality Control in Pharmaceutical Manufacturing +
This track addresses the critical aspects of quality control in pharmaceutical manufacturing processes. Participants will examine regulatory standards and innovative practices that ensure the safety and efficacy of pharmaceutical products.
06 Innovations in Laboratory Diagnostics +
This session will highlight recent innovations in laboratory diagnostics, focusing on technologies that improve diagnostic accuracy and patient outcomes. Discussions will include the role of automation and artificial intelligence in enhancing laboratory efficiency.
07 Sustainable Practices in Pharmacy +
This track will investigate sustainable practices within the pharmacy sector, addressing environmental and economic impacts. Participants will discuss strategies for promoting sustainability in pharmaceutical research and development.
08 Pharmaceutical Trends and Market Dynamics +
This session will analyze current trends in the pharmaceutical industry, including market dynamics and emerging therapeutic areas. Attendees will explore the implications of these trends for research, development, and healthcare delivery.
09 Drug Safety and Pharmacovigilance +
This track will focus on the importance of drug safety and pharmacovigilance in ensuring patient well-being. Participants will discuss methodologies for monitoring adverse drug reactions and the regulatory frameworks that support drug safety.
10 Laboratory Management and Education +
This session will cover essential aspects of laboratory management and education, emphasizing best practices for training and development in laboratory settings. Discussions will include strategies for fostering a culture of continuous improvement and innovation.
11 Molecular Pharmacy and Drug Development +
This track will explore the role of molecular pharmacy in the drug development process, focusing on the design and evaluation of new therapeutic agents. Participants will discuss the integration of molecular techniques in enhancing drug efficacy and safety.