Time |
Topic |
9:00 AM 10:00 AM |
Registration & Networking |
10:00 AM 11:00 AM |
Welcome Address and Conference Inauguration |
|
Technology Trends |
11:00 AM - 12:00 PM |
Panel Discussion - Maximizing Pharma Productivity through Technological Advancement.
- Optimizing formulation process by implementing process analytical technology (PAT) solutions, continuous manufacturing techniques and big data analytics.
- Leveraging AI tools for accelerating drug discovery and development.
- Integrating data analytics tools, advanced spectroscopic and chromatographic techniques for rapid raw material characterization and quality assurance, ensuring consistency and purity.
- Leveraging predictive analytics and AI-driven demand forecasting to optimize inventory, mitigate stock outs, and prevent supply chain disruptions.
- Deploying IoT sensors and blockchain technologies to offer real-time pharmaceutical raw material and finished product tracking and traceability.
Moderator :
Panelists:
- Dr. Andiappan Murugan, Senior Vice President API R&D, Troikaa Pharmaceuticals.
- Dr. Suresh Pathi , Head Operational Excellence-Formulation Cluster, Granules India.
- Ravi Chander Katta , Director - Site Quality Head, Pfizer Vizag.
- Dr. Vellaian Karuppiah , Vice President Operations, Gland Pharma.
|
|
Analytical Advancements |
12:00 PM 12:20 PM |
Revolutionizing Pharma Labs: Advancing Laboratory Practices through Analytical Innovation.
- How cutting-edge technologies such as high-resolution mass spectrometry, next-generation sequencing, and advanced imaging are revolutionizing drug discovery, formulation, and quality control processes in pharmaceutical laboratories.
- Role of AI and ML algorithms in analyzing data, predicting compound properties, and optimizing experiments, speeding-up drug development and assisting in decision-making.
- Emphasize the importance of collaboration between chemists, biologists, pharmacologists, and computational scientists for innovative practices in pharma labs.
- Discover the implementation of robust data systems and laboratory automation.
|
12:20 PM - 12:40 PM |
Partner Session |
|
Impurities Assessment |
12:40 PM - 01:00 PM |
Nitrosamine Contamination in Pharmaceuticals- Risks, Discoveries, and Industry Response.
- Understanding the health risks associated with nitrosamine exposure and their implications.
- Identifying the areas of advancements in analytical techniques for detecting and quantifying nitrosamine impurities.
- Insights on quality control protocols, risk assessment strategies, and collaboration with regulatory agencies to ensure product safety.
|
01.00 PM – 02:00 |
Lunch & Networking |
|
Drugs Repositioning Strategies |
02:00 PM - 02:20 PM |
Fireside Chat : Maximizing Drug Repositioning: India's Strategic Approach to Exploring New Therapeutic Applications
- Insights from Case Studies like Remdesivir etc.
- Benefits of drug repositioning and identifying potential drugs for repurpose.
- Integrating AI into Drug Repositioning Strategies, approaches methods and
consideration.
- Identifying opportunities for cross-sector partnerships and data sharing.
- Understanding regulatory frameworks to support and facilitate drug repositioning
- Discussion of analytical lifecycle management
Moderator :
Panelist :
- Dr. Tathagata Dutta , Chief Technology Officer, JODAS EXPOIM Pharmaceuticals.
- Dr. Srinivas Arutla , Chief Executive Officer, Zenara Pharma.
|
|
Quality Integration in Clinical Development |
02:20 PM - 02:40 PM |
Quality excellence in Clinical Trials
- Quality centric approach in clinical trials- CRO, sponsor and ICH-GCP.
- Audits and inspection readiness in clinical trials.
- Automation in Clinical quality processes.
Dr. Shubhadeep D Sinha , Senior Vice President Development, Hetero Group of Companies (Hetero Labs).
|
|
Pharma Packaging |
02:40 PM - 03:30 PM |
Panel Discussion : Adapting to Evolving Pharmaceutical Packaging Standards
- Understating revised chapters USP 661 and 671compliance and decoding revisions and Strategies to prepare for and adapt to the revised USP standards ahead of the 2025 deadline.
- Overview on technology advancements and how it is facilitating compliance with evolving standards, such as tamper-evident features, serialization, and smart packaging solutions.
- Importance of adapting packaging practices to ensure product safety and integrity, addressing concerns such as counterfeit drugs, contamination, and shelf-life extension.
- Growing importance of sustainable packaging solutions in the pharmaceutical industry and how companies are integrating eco-friendly materials and practices to reduce environmental impact.
- Insights into future trends and advancements in developing flexible and responsive packaging solutions to anticipate regulatory changes and market needs.
Moderator :
Panelist :
Pavankumar Chougule , Head Packaging Development (OSD- Non Sterile), Dr. Reddy's Laboratories.
|
03:30 PM - 03:50 |
Partner Session |
03:50 PM - 04:10 PM |
Tea - Coffee and Networking Break |
|
Pharma Machinery |
04:10 PM – 04:30 PM |
Innovations in Pharmaceutical Machinery: Driving Efficiency and Quality in Drug Manufacturing.
- Understating the need of concept of continuous improvement for designing innovative machinery in pharmaceutical manufacturing.
- Advancements in leak detection technology for pharmaceutical packaging, including non-destructive testing methods and high-speed inspection capabilities.
- Data analytics and machine learning algorithms in optimizing manufacturing processes, predicting equipment failures, and improving overall efficiency.
Dr. Vellaian Karuppiah , Vice President Operations, Gland Pharma.
|
|
Analytical Instrumentation |
04:30 PM - 05:00 PM |
Exploring cutting-edge technologies revolutionizing drug discovery, formulation, and quality control.
- Role of advanced analytics optimizing personalized medicine .
- Leveraging analytics to streamline regulatory processes, accelerate approvals, and bring life-saving therapies to market faster.
- Reducing the complexities of data governance, quality assurance, and regulatory standards with big data.
|
|
End of Day 01 |