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Practical AI for Pharmaceutical Sciences&nbsp;is a hands-on course designed to help pharmacy and life-science professionals understand and apply Artificial Intelligence in real-world pharmaceutical workflows.<ol><li>Learn how to use AI tools to improve research, drug discovery, data analysis, scientific writing, literature review, regulatory work, and everyday productivity—without needing advanced programming skills.</li><li>Through practical examples and industry-focused applications, you’ll learn to turn AI from a concept into a powerful tool for your pharmaceutical career.</li><li>What you’ll gain:</li><li>Learn. Apply. Transform. — Build AI skills for the future of pharma.</li><li><ul><li>Practical AI skills for pharmaceutical sciences</li><li>Real-world use cases and workflows</li><li>AI-assisted research and literature analysis</li><li>Smarter scientific writing and documentation</li><li>AI tools for productivity and data handling</li><li>Career-ready knowledge for the future of pharma</li></ul></li></ol>

Practical AI for Pharmaceutical Sciences

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​ This course gives a practical understanding of how pharmaceutical quality systems are built, implemented and maintained across the product lifecycle. It explains the expectations set by global regulatory bodies and connects them with real operational activities like documentation, deviations, CAPA, change control, validation and audit readiness. Learners will explore the core elements of ICH Q10, along with supporting guidelines such as ICH Q8, Q9 and Q12, to understand how quality works not just as a compliance requirement but as a framework for consistency, patient safety and continuous improvement. By the end of the program, participants will be able to apply quality principles in day-to-day work and contribute meaningfully to a culture of compliance and operational excellence. ​Learning Objectives / Outcomes By the end of this course, participants will be able to understand the structure and purpose of a pharmaceutical quality system and apply regulatory expectations in practical workplace scenarios. They will learn how to manage documentation, deviations, CAPA and change controls in alignment with global standards. They will also gain confidence in reviewing batch records, supporting audits, identifying risks and contributing to continuous improvement initiatives. The course will strengthen their ability to work within GMP environments and support activities across development, manufacturing, testing and lifecycle management. ​Target Audience&nbsp;​ 1)&nbsp;Graduates and postgraduates in pharmacy, biotechnology or life sciences 2)&nbsp;Regulatory, QA, QC and R&amp;D professionals 3)&nbsp;Freshers preparing for entry-level QA or QC roles 4)&nbsp;Professionals interested in operational excellence and compliance ​Course Prerequisites Participants should have a basic understanding of pharmaceutical manufacturing or analytical testing concepts before joining this course. Prior exposure to GMP guidelines, laboratory practices or regulatory terms will be helpful, though not mandatory. The course is suitable for graduates, postgraduates and working professionals from pharmacy, biotechnology, microbiology or related life science fields who want to strengthen their knowledge of quality systems and compliance. Basic computer literacy and the ability to read and interpret technical documentation are expected. ​Instructor Introduction Mr. Dishank Purandare is a graduate with a strong academic and research foundation in computational chemistry, molecular docking, pharmaceutical R&amp;D, and quality sciences. His work focuses on applying in-silico tools to support rational drug design, lead optimization, and mechanism-based evaluation of drug targets.He has authored multiple research publications in reputed journals and is an&nbsp; inventor on granted patents in both the Indian and UK markets. These include innovations related to drug release testing systems, AI-based micro-reactors for nanoparticle synthesis, sensor-based pharmacological evaluation tools, and other applied pharmaceutical technologies. His patent work reflects a consistent integration of computational thinking with experimental and translational research.One of the key research projects involved the&nbsp;design and molecular docking–based evaluation of novel 5-Fluorouracil derivatives targeting thymidylate synthase for non-small cell lung cancer, where docking and structure-based analysis were central to candidate selection and optimization. He also managed and technically guided over 20 projects involving molecular design, docking studies, and computational screening for both academic and industry-oriented research programs.In addition, he has contributed to interdisciplinary innovation through funded projects, including theInnovate H2O grant (Vishnu Foundation TBI and IFIA Bharat)for sustainable management of steroidal drug wastewater, demonstrating&nbsp; ability to translate scientific concepts into real-world solutions.As an instructor, he focuses on making molecular docking practical, structured, and application-driven. This course is designed to help learners understand docking fundamentals, tool selection, workflow design, result interpretation, and common pitfalls, with examples drawn from real research problems. His goal is to equip participants with skills they can confidently apply in drug discovery, academic research, and pharmaceutical R&amp;D environments.

Molecular Docking

Course Description This course gives a practical understanding of how pharmaceutical quality systems are built, implemented and maintained across the product lifecycle. It explains the expectations set by global regulatory bodies and connects them with real operational activities like documentation, deviations, CAPA, change control, validation and audit readiness. Learners will explore the core elements of ICH Q10, along with supporting guidelines such as ICH Q8, Q9 and Q12, to understand how quality works not just as a compliance requirement but as a framework for consistency, patient safety and continuous improvement. By the end of the program, participants will be able to apply quality principles in day-to-day work and contribute meaningfully to a culture of compliance and operational excellence. Learning Objectives / Outcomes By the end of this course, participants will be able to understand the structure and purpose of a pharmaceutical quality system and apply regulatory expectations in practical workplace scenarios. They will learn how to manage documentation, deviations, CAPA and change controls in alignment with global standards. They will also gain confidence in reviewing batch records, supporting audits, identifying risks and contributing to continuous improvement initiatives. The course will strengthen their ability to work within GMP environments and support activities across development, manufacturing, testing and lifecycle management. Target Audience&nbsp;​ 1)&nbsp;Graduates and postgraduates in pharmacy, biotechnology or life sciences 2)&nbsp;Regulatory, QA, QC and R&amp;D professionals 3)&nbsp;Freshers preparing for entry-level QA or QC roles 4)&nbsp;Professionals interested in operational excellence and compliance Course Prerequisites Participants should have a basic understanding of pharmaceutical manufacturing or analytical testing concepts before joining this course. Prior exposure to GMP guidelines, laboratory practices or regulatory terms will be helpful, though not mandatory. The course is suitable for graduates, postgraduates and working professionals from pharmacy, biotechnology, microbiology or related life science fields who want to strengthen their knowledge of quality systems and compliance. Basic computer literacy and the ability to read and interpret technical documentation are expected. Instructor Introduction Mr. Sujith Nair is a distinguished professional with over 20 years of experience in the pharmaceutical industry. A postgraduate in Biotechnology from Mahatma Gandhi University, Kerala, and a graduate in Biotechnology from Mumbai University, Mr. Sujith Nair has established himself as an expert in analytical method development and validation. Driven by a passion for innovation, he specializes in employing the Quality by Design (QbD) approach for method development and is actively engaged in research exploring the intersection of QbD and artificial intelligence. Mr. Sujith Nair is the Founder and Technical Head of SBM PharmaTech, Pune and serves as a Director of Technical Operations at Spectratix Pharma Private Limited, Pune. Beyond his professional pursuits, Mr. Sujith Nair is deeply committed to education and has made it his life’s mission to provide the pharmaceutical industry with highly trained and skilled professionals. His dedication to knowledge sharing is matched by his innovative spirit, reflected in the numerous patents he has under review with the Government of India. He is also the author of the book titled “Quality by Design (QbD) in the Pharmaceutical Industry”.

Pharmaceutical Quality Systems

PharmaGyan Academy