Dispensing Technique in GMP

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• Published on: Dec 16, 2020

Control of Starting Materials in Good Manufacturing Practice

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• Published on: Dec 16, 2020

Control of microorganisms in pharmaceuticals production

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• Published on: Dec 16, 2020

What is analytical method validation in GMP

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• Published on: Dec 16, 2020

Finished Goods Return Procedure in GMP

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• Published on: Oct 16, 2018

How to prepare equipment calibration master plan standard operating procedure

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• Published on: Oct 27, 2017

Aseptic Filling Room Personnel Monitoring

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• Published on: Oct 27, 2017

API Packaging and Labeling Guidelines

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• Published on: Oct 27, 2017

Cleaning Validation for Active Pharmaceutical Ingredients

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• Published on: Oct 27, 2017

How to Prepare SOP for Annual Product Quality Review in GMP

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• Published on: Oct 27, 2017

General Procedure for New Product Registration for Medical Device Site

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• Published on: Oct 27, 2017

Market Actions Policy at a GMP Site

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• Published on: Oct 27, 2017

Disposition of Production Materials and Finished Products at a GMP Site

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• Published on: Oct 27, 2017

Guideline for batch record review of pharmaceuticals and medical devices

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• Published on: Oct 27, 2017

Validation Guideline for Facility and Utility

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• Published on: Oct 27, 2017

Overview of controlling adverse events and product recalls for medical devices

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• Published on: Oct 27, 2017

How to assign expiration date in medicinal products

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• Published on: Oct 27, 2017

Biological test methods validation process in pharmaceuticals

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• Published on: Oct 27, 2017