Blog & Insights
Latest updates and expert analysis from the pharmaceutical industry
FDA Warning — Contaminated Cough Syrups in India
FDA issues warning about contaminated cough syrups found in the Indian market, raising concerns about pharmaceutical quality control.
Cleaning Validation Part 6 — MACO Calculation Limits
Understanding Maximum Allowable Carryover calculations and their role in cleaning validation programs.
Cleaning Validation Part 5 — Surface Area Calculations
Methods for calculating equipment surface area in pharmaceutical cleaning validation.
Cleaning Validation Part 4
Advanced topics in cleaning validation methodology for pharmaceutical manufacturing.
Cleaning Validation Part 3
Sampling strategies and analytical methods for effective cleaning validation.
Information about GSDP and Thermal Mapping
Key information about Good Storage and Distribution Practice and thermal mapping requirements.
Introduction to the Pharmaceutical Industry Workshop
Nippur successfully conducted an introductory workshop on the pharmaceutical industry.
Information About Machine Qualification
Essential information about equipment qualification in pharmaceutical manufacturing.
Cleaning Validation Part 1
Introduction to cleaning validation fundamentals in pharmaceutical manufacturing.