JOB CENTER PR

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Listado de Cursos/Adiestramientos

Unidad De Desarrollo Profesional y Adiestramiento

Quality (Training/Course Programs) List

                      JOB CENTER PR puede desarrollar o proveer el adiestramiento/curso o programa, no limitado a:

  • Certificación en Validación Industrial I- 4 dias
  • Certificación en Validación Industrial II - 4 dias
  • FDA Computer System Validation Certification
  • CAPA and Investigation Training Certification- 3 dias
  • Certificación en Inspector de Calidad
  • cGMPs Trainer Certification Program
  • cGMP for Pharmaceuticals Industry (CFR 21 Part, 210, 211)
  • Buenas Practicas de Laboratorio- No Clinico (GLP)
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820
  • ISO 13485 Regulation Course
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820 for ISO 9000-2000 Certified Organizations 
  • Como escribir efectivamente procedimientos Operacionales (SOP?s) para la Industria Regulada: Farmacéuticas, Biotecnología, Dispositivos Médicos, Planta Química, 2 días
  • Revisión de Lotes (Batch Record Review) 
  • How to Handle Investigations & Deviations
  • How to document and Handling Regulated documentation
  • Quality Assurance Unit: knowing the roles and responsibilities
  • Quality Subsystems: Ensuring Compliance and Product Quality
  • FDA Inspection System Approach and the Consequences of Non-Compliance
  • Internal Auditing for cGMP Compliance I & II
  • Drug Product Submissions for US Regulated Industries
  • Vendor and Contract Supplier Qualification
  • New Drugs Application Submission and Post Approval Changes
  • Post Approval Changes & Change Control
  • Introduction to Regulatory Affairs
  • Quality Assurance in-Process Roles/Manufacturing/Packaging Process
  • Post Approval Changes and Final Product Disposition Roles and Responsibilities
  • Develop, implement and Maintains an Effective CAPA Program
  • Determine the Root Causes and Corrective Action for Product Quality Issues.
  • Audit your CAPA System for FDA Compliance
  • Analytical Problem Solving Techniques / Root Cause Analysis
  • Technical Writing for Compliant Documentation
  • Risk Assessment and Risk Management for Medical & Drug Industry

 


Unidad De Desarrollo Profesional y Adiestramiento

Listado de Cursos/Programas a Ofrecer, no limitado a:

Advance JOB CENTER puede desarrollar o proveer el adiestramiento/curso o programa, no limitado a: 

Quality (Training/Course Programs) List

 CAPA and Investigation Auditor Training Course
cGMP?s Trainer Certification Program
cGMP for Pharmaceuticals Industry (CFR 21 Part, 210, 211)
Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820
ISO 13485 Regulation Course
Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820 for ISO 9000-2000 Certified Organizations 
Como escribir efectivamente procedimientos Operacionales (SOP?s) para la Industria Regulada: Farmacéuticas, Biotecnología, Dispositivos Médicos, Planta Química, 2 días
?Revision de Lotes (Batch Record Review) 
How to Handle Investigations & Deviations
How to document and Handling Regulated documentation
Quality Assurance Unit: knowing the roles and responsibilities
Quality Subsystems: Ensuring Compliance and Product Quality
FDA Inspection System Approach and the Consequences of Non-Compliance
Internal Auditing for cGMP Compliance I & II
Drug Product Submissions for US Regulated Industries
Vendor and Contract Supplier Qualification
New Drugs Application Submission and Post Approval Changes
Post Approval Changes & Change Control
Introduction to Regulatory Affairs
Quality Assurance in-Process Roles/Manufacturing/Packaging Process
Post Approval Changes and Final Product Disposition Roles and Responsibilities
Develop, implement and Maintains an Effective CAPA Program
Determine the Root Causes and Corrective Action for Product Quality Issues.
Audit your CAPA System for FDA Compliance
Analytical Problem Solving Techniques / Root Cause Analysis
Technical Writing for Compliant Documentation
Risk Assessment and Risk Management for Medical & Drug Industry
 

Unidad De Desarrollo Profesional y Adiestramiento

Listado de Cursos/Programas a Ofrecer, no limitado a:

Advance JOB CENTER puede desarrollar o proveer el adiestramiento/curso o programa, no limitado a: 

Quality (Training/Course Programs) List

  •  CAPA and Investigation Auditor Training Course
  • cGMP?s Trainer Certification Program
  • cGMP for Pharmaceuticals Industry (CFR 21 Part, 210, 211)
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820
  • ISO 13485 Regulation Course
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820 for ISO 9000-2000 Certified Organizations 
  • Como escribir efectivamente procedimientos Operacionales (SOP?s) para la Industria Regulada: Farmacéuticas, Biotecnología, Dispositivos Médicos, Planta Química, 2 días
  • ?Revision de Lotes (Batch Record Review) 
  • How to Handle Investigations & Deviations
  • How to document and Handling Regulated documentation
  • Quality Assurance Unit: knowing the roles and responsibilities
  • Quality Subsystems: Ensuring Compliance and Product Quality
  • FDA Inspection System Approach and the Consequences of Non-Compliance
  • Internal Auditing for cGMP Compliance I & II
  • Drug Product Submissions for US Regulated Industries
  • Vendor and Contract Supplier Qualification
  • New Drugs Application Submission and Post Approval Changes
  • Post Approval Changes & Change Control
  • Introduction to Regulatory Affairs
  • Quality Assurance in-Process Roles/Manufacturing/Packaging Process
  • Post Approval Changes and Final Product Disposition Roles and Responsibilities
  • Develop, implement and Maintains an Effective CAPA Program
  • Determine the Root Causes and Corrective Action for Product Quality Issues.
  • Audit your CAPA System for FDA Compliance
  • Analytical Problem Solving Techniques / Root Cause Analysis
  • Technical Writing for Compliant Documentation
  • Risk Assessment and Risk Management for Medical & Drug Industry

 

Unidad De Desarrollo Profesional y Adiestramiento

Listado de Cursos/Programas a Ofrecer, no limitado a:

Advance JOB CENTER puede desarrollar o proveer el adiestramiento/curso o programa, no limitado a: 

Quality (Training/Course Programs) List

  •  CAPA and Investigation Auditor Training Course
  • cGMP?s Trainer Certification Program
  • cGMP for Pharmaceuticals Industry (CFR 21 Part, 210, 211)
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820
  • ISO 13485 Regulation Course
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820 for ISO 9000-2000 Certified Organizations 
  • Como escribir efectivamente procedimientos Operacionales (SOP?s) para la Industria Regulada: Farmacéuticas, Biotecnología, Dispositivos Médicos, Planta Química, 2 días
  • ?Revision de Lotes (Batch Record Review) 
  • How to Handle Investigations & Deviations
  • How to document and Handling Regulated documentation
  • Quality Assurance Unit: knowing the roles and responsibilities
  • Quality Subsystems: Ensuring Compliance and Product Quality
  • FDA Inspection System Approach and the Consequences of Non-Compliance
  • Internal Auditing for cGMP Compliance I & II
  • Drug Product Submissions for US Regulated Industries
  • Vendor and Contract Supplier Qualification
  • New Drugs Application Submission and Post Approval Changes
  • Post Approval Changes & Change Control
  • Introduction to Regulatory Affairs
  • Quality Assurance in-Process Roles/Manufacturing/Packaging Process
  • Post Approval Changes and Final Product Disposition Roles and Responsibilities
  • Develop, implement and Maintains an Effective CAPA Program
  • Determine the Root Causes and Corrective Action for Product Quality Issues.
  • Audit your CAPA System for FDA Compliance
  • Analytical Problem Solving Techniques / Root Cause Analysis
  • Technical Writing for Compliant Documentation
  • Risk Assessment and Risk Management for Medical & Drug Industry

 

Unidad De Desarrollo Profesional y Adiestramiento

Listado de Cursos/Programas a Ofrecer, no limitado a:

Advance JOB CENTER puede desarrollar o proveer el adiestramiento/curso o programa, no limitado a: 

Quality (Training/Course Programs) List

  •  CAPA and Investigation Auditor Training Course
  • cGMP?s Trainer Certification Program
  • cGMP for Pharmaceuticals Industry (CFR 21 Part, 210, 211)
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820
  • ISO 13485 Regulation Course
  • Quality System Regulation (QSR?s) MEDICAL DEVICES, CFR 21, Part 820 for ISO 9000-2000 Certified Organizations 
  • Como escribir efectivamente procedimientos Operacionales (SOP?s) para la Industria Regulada: Farmacéuticas, Biotecnología, Dispositivos Médicos, Planta Química, 2 días
  • ?Revision de Lotes (Batch Record Review) 
  • How to Handle Investigations & Deviations
  • How to document and Handling Regulated documentation
  • Quality Assurance Unit: knowing the roles and responsibilities
  • Quality Subsystems: Ensuring Compliance and Product Quality
  • FDA Inspection System Approach and the Consequences of Non-Compliance
  • Internal Auditing for cGMP Compliance I & II
  • Drug Product Submissions for US Regulated Industries
  • Vendor and Contract Supplier Qualification
  • New Drugs Application Submission and Post Approval Changes
  • Post Approval Changes & Change Control
  • Introduction to Regulatory Affairs
  • Quality Assurance in-Process Roles/Manufacturing/Packaging Process
  • Post Approval Changes and Final Product Disposition Roles and Responsibilities
  • Develop, implement and Maintains an Effective CAPA Program
  • Determine the Root Causes and Corrective Action for Product Quality Issues.
  • Audit your CAPA System for FDA Compliance
  • Analytical Problem Solving Techniques / Root Cause Analysis
  • Technical Writing for Compliant Documentation
  • Risk Assessment and Risk Management for Medical & Drug Industry

 

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  • "Lo mas que me gusto del curso fue la explicacia exacta y detallada de todos los subtemas dentro de las presentaciones. Tambien la disponibilidad 24/7 del curso online. FDA In..."
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