A properly-composed JHA/AHA is one of the primary documents that large clients are increasingly asking to review in adva...
Using a library of SOP’s to help organize and control your operations is just good business sense. This is particu...
Counterfeit drugs pose a public health hazard, waste consumer income, and reduce the incentive to engage in research and...
Regulatory strategy in the pharmaceutical industry refers to the plan put in place by a pharmaceutical company to ensure...
In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect of ma...
The price of medicines is one of the factors that can limit the affordability of medicines to the population. So there...
This course provides guidance on how to perform QC analytical test method validations and transfers. One of the most cri...
This webinar gives a fundamental knowledge of stability testing requirements for establishing storage conditions and exp...
Compliance under GLP can be difficult. The setting up of a system to monitor the performance of methods and instruments...
The records in a lab – the logbooks for chemicals, reagents, and calibration solutions, sample preparation, instru...
Accuracy, the ability of a methodology to give results within acceptable limits when compared to known values, is a fund...
Assessment of the cause for non-compliance is a structured series of branching questions. The answers to these eliminate...
Low-level compound analysis has many differences from that of the more common analyses aimed at major components. The re...
Regulatory inspections are the end result of the Company QMS assessment. Companies and Sponsors of trials need to have p...
Participants will be introduced to biopharmaceutic and pharmacokinetic principles that can be applied to systemic drug a...
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