Hybrid Conference (In Person / Virtual)

International Conference on Industrial Pharmacy and Applications (ICIPA - 27)
8th - 9th March 2027 , Beirut, Lebanon
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Conference Notifications:

"Be sure to check this section regularly for all IIRD Global Conference updates. We’ll keep you informed about deadlines, event details, and more important notifications."

  • Abstract Submissions Open:
    "We are now accepting abstract submissions for the IIRD Global Conference in Beirut. Submit your abstract by today to be part of this exciting international event." Call for Abstracts – Submit Now!
  • Paper Submission Guidelines:
    "Please ensure your paper follows the submission guidelines for smooth processing. Visit our paper submission page for more details."
  • Peer Review Process:
    "The peer review process will begin soon. Authors will receive valuable feedback that will help enhance their presentations for the Beirut conference."
  • Networking with Global Experts:
    "Join global experts at our conference in Beirut and engage in meaningful conversations. Build relationships that last." Register now to join!
  • Best Paper Presentation Award:
    Dr. Shatha Hawarna from Hamdan Bin Mohammed Smart University received the Best Paper Presentation Award at (ICBAI-25) in Bangkok, Thailand.
  • SDG-Inspired Conference Focus:
    "The conference will explore themes related to sustainability and inclusive development, with an emphasis on research that contributes to global well-being."

Conference Session Tracks

SDG Wheel

Aligned with

UN Sustainable Development Goals

This conference contributes to global sustainability by aligning its research discussions and academic sessions with key United Nations Sustainable Development Goals. It fosters knowledge exchange, innovation, and collaborative engagement.

SDG 3 SDG 3 — Good Health and Well-being
SDG 4 SDG 4 — Quality Education
SDG 8 SDG 8 — Decent Work and Economic Growth
Session Tracks
Track 01
Innovations in Drug Discovery and Development

This track focuses on the latest advancements in drug discovery methodologies and development processes. It aims to explore novel approaches that enhance the efficacy and safety of pharmaceutical products.

Track 02
Industrial Pharmaceutics: Challenges and Solutions

This session addresses the complexities of industrial pharmaceutics, including formulation, manufacturing, and quality control. Participants will discuss innovative techniques to overcome common challenges in the production of pharmaceutical products.

Track 03
Pre-Clinical Studies: Bridging Bench to Bedside

This track highlights the importance of pre-clinical studies in the drug development pipeline. It aims to present methodologies that effectively translate laboratory findings into clinical applications.

Track 04
Pharmacovigilance and Clinical Trials

This session examines the critical role of pharmacovigilance in ensuring drug safety during clinical trials. Discussions will include regulatory requirements and best practices for monitoring adverse drug reactions.

Track 05
Clinical Studies: Design and Implementation

This track focuses on the design and execution of clinical studies, emphasizing statistical methodologies and ethical considerations. It aims to share insights on optimizing study protocols for better outcomes.

Track 06
Supply Chain Management in Pharmaceuticals

This session explores the intricacies of supply chain management within the pharmaceutical industry. Topics will include logistics, inventory control, and strategies for ensuring a consistent supply of quality products.

Track 07
Waste Management in Pharmaceutical Production

This track addresses the environmental challenges associated with pharmaceutical waste management. Participants will discuss sustainable practices and regulatory compliance in waste disposal.

Track 08
Product Management in the Pharmaceutical Sector

This session focuses on the strategic aspects of product management in pharmaceuticals, including lifecycle management and market analysis. It aims to provide insights into effective product positioning and commercialization.

Track 09
Post-Marketing Surveillance: Ensuring Drug Safety

This track emphasizes the importance of post-marketing surveillance in monitoring drug safety and efficacy after market release. Discussions will include methodologies for collecting and analyzing post-marketing data.

Track 10
Good Manufacturing Practices: Ensuring Quality

This session delves into the principles of Good Manufacturing Practices (GMP) and their application in the pharmaceutical industry. Participants will explore case studies that highlight the impact of GMP on product quality.

Track 11
Patent Applications and Drug Registration

This track focuses on the legal and regulatory aspects of patent applications and drug registration processes. It aims to provide insights into navigating the complexities of intellectual property in pharmaceuticals.

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