GMP Compliance: Introduction
Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food
Practical Computerized and Automated System Validation
Two Days Training Session By discussing Patient Risk-based Approach, this Training session focuses on developing and implementing regulated digital and
Production Value and Overall Equipment Effectiveness
Overall Equipment Effectiveness (OEE) is a well-established KPI metrics to measure the equipment effectiveness. OEE has been widely used for
Data Quality and Integrity Management in GMP Environment
Description: Data management refers to all activities performed during data lifecycle including but not limited to data policy, documentation, quality,
Introduction to EU GMP Annex 11
The EU GMP Annex 11 applies to all forms of computerized systems used as part of a GMP regulated activities.
Digital & Computerized System Validation
The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well
Lean Cleaning Validation
Description: Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),
GACP and GMP for Cannabis products
Description: Good agricultural practices (GACP) and good manufacturing practices (GMP) for Cannabis and Cannabis-derived products training session is intended for
Gestion de la Qualité du Cannabis
La gestion de qualité au sein des entreprises est une activité cruciale qui a un impact sur l’efficacité, la qualité,
GMP Compliance: Introduction
Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food
Production Value and Overall Equipment Effectiveness
Overall Equipment Effectiveness (OEE) is a well-established KPI metrics to measure the equipment effectiveness. OEE has been widely used for
Data Quality and Integrity Management in GMP Environment
Description: Data management refers to all activities performed during data lifecycle including but not limited to data policy, documentation, quality,
Introduction to EU GMP Annex 11
The EU GMP Annex 11 applies to all forms of computerized systems used as part of a GMP regulated activities.
Digital & Computerized System Validation
The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well
Lean Cleaning Validation
Description: Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),
GACP and GMP for Cannabis products
Description: Good agricultural practices (GACP) and good manufacturing practices (GMP) for Cannabis and Cannabis-derived products training session is intended for
Gestion de la Qualité du Cannabis
La gestion de qualité au sein des entreprises est une activité cruciale qui a un impact sur l’efficacité, la qualité,
GMP Compliance: Introduction
Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food
Practical Computerized and Automated System Validation
Two Days Training Session By discussing Patient Risk-based Approach, this Training session focuses on developing and implementing regulated digital and
Production Value and Overall Equipment Effectiveness
Overall Equipment Effectiveness (OEE) is a well-established KPI metrics to measure the equipment effectiveness. OEE has been widely used for
Data Quality and Integrity Management in GMP Environment
Description: Data management refers to all activities performed during data lifecycle including but not limited to data policy, documentation, quality,
Introduction to EU GMP Annex 11
The EU GMP Annex 11 applies to all forms of computerized systems used as part of a GMP regulated activities.
Digital & Computerized System Validation
The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well
Lean Cleaning Validation
Description: Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),
GACP and GMP for Cannabis products
Description: Good agricultural practices (GACP) and good manufacturing practices (GMP) for Cannabis and Cannabis-derived products training session is intended for
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