by maheshbhuva | Jun 28, 2026 | Uncategorized
product dimensions. For e-cigarettes, manufacturers would also need to provide specifications such as e-liquid volume, battery capacity, and wattage. To streamline and increase efficiency, in most cases manufacturers would be required to submit information...
by maheshbhuva | Jun 28, 2026 | Uncategorized
Emperor Palpatine has announced open elections for a new Emperor — and he’s nominated Darth Vader. You get to nominate one challenger. Share this: Share on Facebook (Opens in new window) Facebook Email a link to a friend (Opens in new window) Email Share on Reddit... by maheshbhuva | Jun 15, 2026 | Analytical Chemistry, Documents error (DIN), Out of specification, Pharmaceutical interview,, QMS, Quality control (QC)
RCA (ROOT CAUSE ANALYSIS) IN PHARMACEUTICAL INDUSTRIES AS PER REGULATORY REQUIREMENTS 1. PROBLEM IDENTIFICATION What Happens Clearly define the deviation, OOS, OOT, complaint, breakdown, audit observation, or incident. Includes Deviation description Date & time... by maheshbhuva | Jun 13, 2026 | Analytical Chemistry, Newsletter, Nitrosamine, Quality control (QC)
* Nitrosamines are trace chemical impurities. * They are classified as probable human carcinogens. * Global agencies require a strict 3-step risk assessment framework. * Manufacturers must evaluate, test, and fix any impurity risks.1. The Global CPCA SystemAgencies... by maheshbhuva | Jun 10, 2026 | Analytical Chemistry, Analytical method development hplc,, Method validation, Quality control (QC)
Specificity This concept is essential in scientific analysis. When you create a method to measure something (like a drug or a chemical), you must prove that the method only measures that specific substance and isn’t being ‘fooled’ by other things in...