'Batch record' diaporamas de présentation

ICH Q7A GMP Guidance For API

ICH Q7A GMP Guidance For API. Good Documentation Practices. Why Documentation is required..?. To define the method and control To prevent errors from spoken communication. Click for Example. This section covers. Documentation System and Specifications Equipment Cleaning and Use Record

395 views • 38 slides

2.78k views • 31 slides

315 views • 31 slides

Basic Principles of GMP

Basic Principles of GMP. Documentation - Part 1. Workshop on GMP and Quality Assurance of HIV products Shanghai, China 28 Feb - 4 March 2005 Maija Hietava M.Sci.Pharm Quality Assurance and Safety: Medicines, Medicines Policy and Standards, Health Technology and Pharmaceuticals Cluster

606 views • 15 slides

Batch Record Management System

In the pharmaceutical industry, there are various types of data that are needed to be recorded. Traditionally, pharmaceutical industries use paper to maintain Batch Records like Batch Manufacturing Records (BMR), BPR, process and equipment templates, etc.

1.06k views • 1 slides