The Pharmaceutical Blog are organised into five core categories:
Founded by industry veteran Dr. Pramod Kumar Pandey, PharmaGuru provides practical, industry-focused pharmaceutical training designed to help professionals at every career stage—from beginners and students to experienced chemists, researchers, managers, general managers, leaders, directors, and academicians—develop practical, job-ready skills.
Our pharmaceutical courses cover key areas of the pharmaceutical industry, including Analytical Research and Development (AR&D), Quality Control (QC), Quality Assurance (QA), Regulatory Affairs, Good Laboratory Practices (GLP), Analytical Method Development, Analytical Method Validation, HPLC, GC, LC-MS, GC-MS, Pharmaceutical Impurities, Stability Studies, & CAPA management.
Whether you are a pharmaceutical student starting your career, a laboratory chemist developing analytical expertise, a researcher working in pharmaceutical R&D, a QC/QA professional, or an experienced manager or leader, PharmaGuru offers industry-oriented pharmaceutical training to support your professional development.
Our goal is simple: turn pharmaceutical knowledge into practical skills that can be applied in real-world pharmaceutical laboratories, R&D environments, quality functions, and regulatory operations.
Dr. Pramod Kumar Pandey is a seasoned Analytical Research Expert with over 31 years of experience in the pharmaceutical industry, having worked with leading Indian and global pharmaceutical companies. Throughout his career, he has successfully navigated major regulatory audits, including USFDA, KFDA, EMA, Health Canada, PMDA, and ANVISA, demonstrating extensive expertise in regulatory compliance, analytical research, and quality standards.
As the Founder of PharmaGuru, Dr. Pandey is dedicated to empowering pharmaceutical professionals through practical training and knowledge sharing. His mission is to bridge the gap between theoretical knowledge and real-world industry practices, helping professionals strengthen their skills in analytical research, quality control, and regulatory compliance
Impurity Control Strategies (chiral, achiral, metal, genotoxins, etc.), Chiral Separation,
Analytical Method Development, Analytical Method Validation, GLP (SOP, STP, Monograph, OOS,
OOT, CAPA and LIR, etc.), Stability Studies, Audit Management, Training, Troubleshooting,
Handling Regulatory Query, Standard/Impurity Characterisation, and Analytical Techniques
(HPLC, GC, GC-MS, LC-MS, Spectroscopic Techniques and Chemical Techniques)
Process for purifying Varenicline L-tartrate salt and preparing crystalline forms of
Varenicline L-tartrate salt (Pub No.:US2010/0010221A1, Date Jan.14, 2010) Process for
purifying Varenicline L-tartrate salt and preparing crystalline forms of Varenicline
L-tartrate salt (Pub No.: US2010/0010221A1, Date Jan.14, 2010)
“Our Mission is to train pharmaceutical professionals by transferring skill-based knowledge through regular blogs, trainings and courses”
“Our Vision is to equip pharmaceutical professionals around the world with skill-based knowledge to make them more Innovative and Successful”
Quick Links