Prashant Sir official
FOR Pharma, Nutraceutical, Food and related PROFESSIONAL,
CHANGE CONTROL. (Change Management in Pharmaceutical QA)
RBI CDSCO (Risk-Based Inspection)
BALANCE CALIBRATION
NITROSAMINE IMPURITIES (Risk, Regulation & Mitigation Explained)
Top 10 Common Mistakes in Audit CAPA Response | How to Avoid CAPA Pitfalls.
Continuous Process Verification (CPV)
D & C ACT SESSION 3 : SCHEDULES
D & C ACT SESSION 2: SCHEDULES
DRUG & COSMETIC ACT- SESSION 1 (GMP Evolution Unveiled: Key Terms in the D & C Act)
Rounding off & Significant Figure in Pharma
Tablet defects Causes and Remedies. (Compression defects and coating defects).
Cleaning validation Part 7 Recovery study
Bracketing and matrixing in stability studies
Stability Studies In Pharmaceutical & Food Industry
Punches and Dies of Tablet Press (Compression Machine) B or D Tooling, BB or DB tooling.
How to deal with change in life & at work.
FDA 483
RECAP OF ALL VIDEOS ON VALIDATION QUALIFICATION UTILITY GMP GLP
MEDIA FILLS - ASEPTIC PROCESS SIMULATION STUDY
Temperature Mapping or Temperature Profiling in Pharma.
QR Code, Data Matrix code, Bar code: Differences and usage
Assigning Expiry date, Shelf life, retest date
Difference between Shelf Life, Expiry date, Use before, Best before, use by date.
Cleaning validation PART 6 - Analytical method validation. AMV
Cleaning validation :HOLD TIME STUDY ( Part 5)
Cleaning validation Part 4- MACO CALCULATIONS
Worst cases in Cleaning validation #MACO #PDE #ADE #LD50 #MAC #MSR
CLEANING VALIDATION- PART 2 : PROTOCOL & REPORT
CLEANING VALIDATION PART 1: BASIC UNDERSTANDING
Water for Pharmaceutical Use