Lean Cleaning Validation
Description: Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),
QC Lab Equipment Qualification and Data Integrity
Objectives Analytical equipment and instruments provide important scientific data about manufactured products that serves to ensure that they meet specifications.
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
Practical HACCP for Drug and Food Safety
This 4-hour interactive online workshop will enable participants to develop practical knowledge of the principles of HACCP for Drug and
Successful Implementation of Data Integrity
Successful Implementation of Data Integrity into Pharmaceutical Quality System – In recent years, US FDA, MHRA, EU GMP, WHO, and Health
Best Practices of Quality Risk Management
Quality Risk Management (QRM) principles require the evaluation of risk to patient safety and product quality based on scientific knowledge,
Lean Six Sigma Yellow Belt Certification Exam Prep Training
3 Days Classroom Certification – Objectives: Our Yellow Belt Lean Six Sigma Training Content is an assembly of a comprehensive
Risk-based Continued Process Verification
Objectives: The third phase of the process validation life cycle, continued process verification, is the ongoing assurance that the routine
Travailler dans un environnement BPF
Objectifs: Revoir les réglementations récentes BPF applicables aux produits cosmétiques, de santé naturels, pharmaceutiques, et alimentaires. Ce cours offre une
GMP Compliance: Introduction
Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food
Introduction to USFDA 21 CFR Part 11
The 21 cfr part 11 applies to records in electronic form that are created, modified, maintained, archived, retrieved, or transmitted,
Lean Cleaning Validation
Description: Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),
QC Lab Equipment Qualification and Data Integrity
Objectives Analytical equipment and instruments provide important scientific data about manufactured products that serves to ensure that they meet specifications.
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
Practical HACCP for Drug and Food Safety
This 4-hour interactive online workshop will enable participants to develop practical knowledge of the principles of HACCP for Drug and
Successful Implementation of Data Integrity
Successful Implementation of Data Integrity into Pharmaceutical Quality System – In recent years, US FDA, MHRA, EU GMP, WHO, and Health
Best Practices of Quality Risk Management
Quality Risk Management (QRM) principles require the evaluation of risk to patient safety and product quality based on scientific knowledge,
Lean Management et Lean Six Sigma Ceinture Blanche
Objectifs: Comprendre les bénéfices de cette méthode reconnue, maîtriser le rôle et les responsabilités de chacun des acteurs de l’amélioration
Risk-based Continued Process Verification
Objectives: The third phase of the process validation life cycle, continued process verification, is the ongoing assurance that the routine
Travailler dans un environnement BPF
Objectifs: Revoir les réglementations récentes BPF applicables aux produits cosmétiques, de santé naturels, pharmaceutiques, et alimentaires. Ce cours offre une
GMP Compliance: Introduction
Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food
Introduction to USFDA 21 CFR Part 11
The 21 cfr part 11 applies to records in electronic form that are created, modified, maintained, archived, retrieved, or transmitted,
Lean Cleaning Validation
Description: Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),
QC Lab Equipment Qualification and Data Integrity
Objectives Analytical equipment and instruments provide important scientific data about manufactured products that serves to ensure that they meet specifications.
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
Practical HACCP for Drug and Food Safety
This 4-hour interactive online workshop will enable participants to develop practical knowledge of the principles of HACCP for Drug and
Successful Implementation of Data Integrity
Successful Implementation of Data Integrity into Pharmaceutical Quality System – In recent years, US FDA, MHRA, EU GMP, WHO, and Health
Best Practices of Quality Risk Management
Quality Risk Management (QRM) principles require the evaluation of risk to patient safety and product quality based on scientific knowledge,
Lean Management et Lean Six Sigma Ceinture Blanche
Objectifs: Comprendre les bénéfices de cette méthode reconnue, maîtriser le rôle et les responsabilités de chacun des acteurs de l’amélioration
Lean Six Sigma Yellow Belt Certification Exam Prep Training
3 Days Classroom Certification – Objectives: Our Yellow Belt Lean Six Sigma Training Content is an assembly of a comprehensive
Risk-based Continued Process Verification
Objectives: The third phase of the process validation life cycle, continued process verification, is the ongoing assurance that the routine
Travailler dans un environnement BPF
Objectifs: Revoir les réglementations récentes BPF applicables aux produits cosmétiques, de santé naturels, pharmaceutiques, et alimentaires. Ce cours offre une
GMP Compliance: Introduction
Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food
Introduction to USFDA 21 CFR Part 11
The 21 cfr part 11 applies to records in electronic form that are created, modified, maintained, archived, retrieved, or transmitted,