PharmaGuru Huda Sector, Faridabad, Haryana

Fundamentals of HPLCGrasp the principles of how liquid chromatography separates compounds via a liquid mobile phase and a solid stationary phase, focusing on different ≤RP‑HPLC and other modes. Fundamentals of HPLCGrasp the principles of how liquid chromatography separates compounds via a liquid mobile phase and a solid stationary phase, focusing on different ≤RP‑HPLC and other modes. Choosing the Right Mode and ComponentsLearn how to select the appropriate HPLC mode (e.g., reverse-phase, normal-phase, size-exclusion, affinity), together with the right column chemistry and mobile phase for specific analytes. Optimising Method ParametersDive into optimising HPLC conditions—flow rate, temperature, mobile phase composition, and detection settings—to balance resolution, run time, and reproducibility. Method Validation EssentialsUnderstand how to validate your HPLC method using parameters like specificity, linearity, accuracy, precision, detection limits, and robustness. Impurity Detection & Stability TestingUse HPLC for impurity profiling, degradation product analysis, and stability studies—key for ensuring drug quality throughout shelf life. Applications Across the Product LifecycleDiscover how HPLC supports drug development—from screening in discovery, through formulation studies and ADME (absorption, distribution, metabolism, excretion) profiling, to quality control of finished products. Regulatory and Quality ComplianceLearn about the importance of regulatory alignment (FDA, EMA, ICH), system suitability tests, documentation, and data integrity in HPLC workflows. Emerging Techniques & InnovationsGet introduced to advanced methods like UHPLC, hyphenated techniques (e.g., LC‑MS), monolithic columns, and emerging trends such as automation, green chemistry, and microfluidics.

PharmaGuru.co provides online training program on the following courses: Step-by-Step Analytical Method Validation Step-by-Step Guide to HPLC Method Development Step-by-Step Guide to GC Method Development Step by Step Chiral Method Development QBD approach in Control of Pharmaceutical Impurities Step-by-Step Guide to LCMS Method Development Step-by-Step Guide to GCMS Method Development Validation and Verification of Analytical Method Forced Degradation Study and Photo Stability RFT Approach in Technology Transfer of Analytical Method QBD approach in Pharmaceutical method development QBD approach in Control of Pharmaceutical Impurities Potency, Purity and Assay in Pharmaceutical Analysis Pharma Interview Preparation Guide to Effective CAPA Management Basic FDA GLP Training GMP (Good Manufacturing Practices in Pharmaceuticals Avoiding Pharmaceutical Data Integrity Problems Handling OOS, OOT and completing the investigation report Stability Testing Role of RRF in the im Related substances test SOP: How to Write and Implement IQ, OQ and PQ How to handle an FDA Audit? How to define pharmaceutical specifications Analytical Techniques used in Pharmaceutical Analysis