The Complete Pharmaceutical Production Course 2025 Day-1: Introduction to Pharma Industry-Types of formulations Day-2: USFDA Guidelines to be followed and their importance in industry. Day-2: USFDA Guidelines to be followed and their importance in industry. Day-3: cGMP regulations Day-4: Good documentation practices, Data Integrity and ALCOA Principles Day-5: Importance of Line clearance procedures Day-6: Introduction to manufacturing of APIs Day-7: Discussion on various equipment’s used in manufacture of APIs—session1. Day-8: Discussion on various equipment’s used in manufacture of APIs—session2. Day-9: Manufacturing process of APIs Day-10: Introduction to manufacturing of OSDs Day-11: Discussion on various equipment’s used in manufacture of OSDs—session1. Day-12: Discussion on various equipment’s used in manufacture of OSDs—session2. Day-13: Granulation processes Day-14: Manufacturing process of Tablets Day-15: Manufacturing process of liquids and semisolids Day-16: Manufacturing process of capsules Day-17: Introduction to manufacturing of sterile formulations, Discussion on clean room conditions Day-18: Discussion on various equipment’s used in manufacture of steriles Day-19: Manufacturing process of various sterile formulations Day-20: Introduction to packing of various formulations. Day-21: Discussion on various equipment’s used for packing Day-22: Discussion on various checkpoints during packing Day-23: Role and importance of IPQA in the manufacturing and packing. Day-24: Batch release procedure into market