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This document outlines a Live Online Training program focused on the Impurities Workshop, providing training on general strategies for the identification and control of impurities, nitrosamine impurities, and elemental impurities, scheduled from 18 to 20 November 2025. It includes objectives, background, target audience, and detailed program information for each part of the workshop.
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How to fill out gmp certification programme

01
Identify the relevant GMP guidelines for your industry.
02
Gather necessary documentation related to your processes and procedures.
03
Train employees on GMP principles and practices.
04
Perform a gap analysis to identify areas needing improvement.
05
Implement corrective actions for any deficiencies found.
06
Conduct internal audits to ensure compliance with GMP standards.
07
Prepare the required application forms for certification.
08
Submit the application along with supporting documentation to the certifying body.
09
Cooperate with the certifying body during their evaluation process.
10
Address any findings from the certification audit before final approval.

Who needs gmp certification programme?

01
Manufacturers in the pharmaceutical industry.
02
Food and beverage companies.
03
Medical device producers.
04
Cosmetic manufacturers.
05
Any organization aiming to ensure product safety and quality.
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The GMP (Good Manufacturing Practices) certification programme is a system that ensures products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in pharmaceutical production that cannot be eliminated through testing the final product.
Manufacturers of pharmaceutical products, food ingredients, dietary supplements, and any other goods subject to health regulations are typically required to comply with and file for GMP certification.
To fill out the GMP certification programme, manufacturers need to complete an application, provide documentation regarding their quality management system, safety procedures, and operational processes, and submit reports or evidence demonstrating compliance with GMP standards.
The purpose of the GMP certification programme is to ensure that products are produced in a quality environment, reducing the risk of contamination, errors, and defects, thereby ensuring that the end products are safe for consumption.
Information that must be reported includes detailed descriptions of production processes, outcomes of quality control tests, documentation of equipment maintenance, training records of personnel, and any incidents of non-compliance or quality issues.
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