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Siedlerstraße 7 | 68623 Lampertheim, Deutschland

info@zamann-pharma.com

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Wir begleiten Sie auf Ihrer Qualitätsreise 

Mit Zamann haben Sie einen Partner an Ihrer Seite, der sich darauf konzentriert, Ihr Unternehmen mithilfe von Qualitätsberatung, Digitalisierung, globalem Projektmanagement sowie Validierung und Qualifizierung auf neue Höhen zu bringen. 

"Die Gewährleistung von Patientensicherheit, Einhaltung von behördlichen Anforderungen und die Kostensenkung stehen im Mittelpunkt unserer Lösungen.” 

Unsere Dienstleistungen

  • Digital Solutions (Computerized Systems) – Implementation and Improvements

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  • Digital Solutions (Computerized Systems) – Routine Support

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  • Quality Systems – Implementation and Improvement

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  • Quality Systems – Routine Support

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  • Qualification and Validation – Implementation and Improvement

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  • Qualification and Validation – Routine Support

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  • Computerized Systems Validation Landscape – Implementation or Improvement

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  • Master Data Management (Computerized Systems) – Strategic Consultancy

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  • Access Management (Computerized Systems) – Strategic Consultancy

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  • Implementation of a new Computerized System – Strategic Consultancy

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  • Computerized Systems Validation Audit Readiness – Strategic Consultancy

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  • Master Data Management (Computerized Systems) – Routine Support

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  • Access Management (Computerized Systems) – Routine Support

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  • Computerized Systems Validation – Routine Support

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  • Computerized Systems Validation Audit Readiness – Routine Support

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  • Quality Management Systems Landscape – Implementation or Improvement

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  • Knowledge Management – Strategic Consultancy

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  • Non-compliance – Strategic Consultancy

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  • Change Control – Strategic Consultancy

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  • Risk Management – Strategic Consultancy

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  • Market Complaints – Strategic Consultancy

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  • Quality Management Review Support

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  • Batch Record Review – Strategic Consultancy

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  • Periodical Internal Audits – Strategic Consultancy

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  • EudraLex Vol.4 Annex 1 – Strategic Consultancy

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  • Project Management with Quality Focus – Strategic Consultancy

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  • Quality Management Systems Audit Readiness – Strategic Consultancy

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  • Knowledge Management – Routine Support

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  • Non-compliance – Routine Support

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  • Change Control – Routine Support

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  • Risk Management – Routine Support

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  • Market Complaints – Routine Support

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  • Batch Record Review – Routine Support

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  • Periodical Internal Audits – Routine Support

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  • EudraLex Vol.4 Annex 1 – Routine Support

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  • Project Management with Quality Focus – Routine Support

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  • Quality Management Systems Audit Readiness – Routine Support

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  • Equipment Qualification – Strategic Consultancy

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  • Cleaning Validation – Strategic Consultancy

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  • Process Validation – Strategic Consultancy

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  • Water Systems Validation (WFI, PW and Pure Steam) – Strategic Consultancy

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  • Equipment Qualification – Routine Support

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  • Cleaning Validation – Routine Support

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  • Process Validation – Routine Support

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  • Water Systems Validation (WFI, PW and Pure Steam) – Routine Support

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  • Computerized Systems Validation Landscape – Strategy Definition

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  • Computerized Systems Validation Landscape – Operational Documents Creation

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  • Computerized Systems Validation Landscape – GAP Assessment

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  • Master Data Management (Computerized Systems)– Strategy Definition

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  • Master Data Management (Computerized Systems) – GAP Assessment

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  • Access Management (Computerized Systems) – Strategy Definition

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  • Access Management (Computerized Systems) – GAP Assessment

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  • New Computerized System – Support on Implementation

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  • Labware LIMS System – Implementation Support

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  • Computerized Systems Implementation – Project Management with Quality Focus

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  • Waters Empower System – Implementation Support

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  • e-QMS System – Implementation Support

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  • Computerized Systems Validation Audit Readiness – Strategy Definition

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  • Computerized Systems Validation Audit Readiness – GAP Assessment

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  • Master Data Management (Computerized Systems) – Audit Execution

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  • Master Data Management (Computerized Systems) – Workshop and Trainings

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  • Access Management (Computerized Systems) – Audit Execution

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  • Access Management (Computerized Systems) – Workshop and Trainings

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  • Computerized Systems Validation – Execution

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  • Computerized Systems Validation – Periodic Review Execution

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  • Computerized Systems Validation – Audit Trail Review Execution

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  • Labware LIMS System – Routine Support

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  • Waters Empower System – Routine Support

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  • e-QMS System – Routine Support

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  • Computerized Systems Validation – Workshop and Trainings

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  • Computerized Systems Validation Audit Readiness – CAPA Plan Management

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  • Computerized Systems Validation Audit Readiness – Audit Execution

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  • Computerized Systems Validation Audit Readiness – Workshop and Trainings

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  • Quality Management Systems Landscape – Strategy Definition

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  • Quality Management Systems Landscape – Operational Documents Creation

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  • Quality Management Systems Landscape – GAP Assessment

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  • Knowledge Management – Strategy Definition

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  • Knowledge Management – GAP Assessment

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  • Non-compliance – Strategy Definition

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  • Non-compliance – GAP Assessment

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  • Change Control – Strategy Definition

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  • Change Control – GAP Assessment

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  • Risk Management – Strategy Definition

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  • Risk Management – GAP Assessment

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  • Market Complaints – Strategy Definition

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  • Market Complaints – GAP Assessment

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  • Quality Management Review – Strategy Definition

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  • Quality Management Review – GAP Assessment

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  • Batch Record Review – Strategy Definition

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  • Batch Record Review – GAP Assessment

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  • Periodical Internal Audits – Strategy Definition

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  • Periodical Internal Audits – GAP Assessment

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  • EudraLex Vol.4 Annex 1 – Strategy Definition

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  • EudraLex Vol.4 Annex 1 – GAP Assessment

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  • Project Management with Quality Focus – Strategy Creation

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  • Project Management with Quality Focus – GAP Assessment

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  • QMS Audit Readiness – Strategy Definition

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  • QMS Audit Readiness – Full Program Implementation

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  • Knowledge Management – General GxP Trainings Program

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  • Knowledge Management – Focused Trainings

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  • Non-compliance – Audit Execution

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  • Non-compliance – Workshop and Trainings

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  • Change Control – Audit Execution

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  • Change Control – Workshop and Trainings

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  • Risk Management – Audit Execution

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  • Risk Management – Workshop and Trainings

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  • Market Complaints – Audit Execution

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  • Market Complaints – Workshop and Trainings

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  • Batch Record Review – Execution

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  • Batch Record Review – Workshop and Trainings

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  • Periodical Internal Audits – Execution

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  • Periodical Internal Audits – CAPA Plan Management

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  • Periodical Internal Audits – Workshop and Trainings

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  • EudraLex Vol.4 Annex 1 – Project Management

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  • EudraLex Vol.4 Annex 1 – Workshop and Trainings

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  • Project Management with Quality Focus – Execution

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  • Management of GxP Projects – Workshop and Trainings

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  • QMS Audit Readiness – GxP Audit Execution

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  • QMS Audit Readiness – Workshop and Trainings

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  • QMS Audit Readiness – CAPA Plan Management

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  • Equipment Qualification – Strategy Definition

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  • Equipment Qualification – Operational Documents Creation

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  • Equipment Qualification – GAP Assessment

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  • Cleaning Validation – Strategy Definition

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  • Cleaning Validation – Operational Documents Creation

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  • Cleaning Validation – GAP Assessment

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  • Process Validation – Strategy Definition

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  • Process Validation – Operational Documents Creation

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  • Process Validation – GAP Assessment

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  • Water Systems Validation (WFI, PW and Pure Steam) – Strategy Definition

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  • Water Systems Validation (WFI, PW and Pure Steam) – Operational Documents Creation

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  • Water Systems Validation (WFI, PW and Pure Steam) – GAP Assessment

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  • Equipment Qualification – Execution

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  • Equipment Qualification – Project Management

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  • Equipment Qualification – Workshop and Trainings

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  • Cleaning Validation – Execution (Equipment and Lab Glassware)

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  • Cleaning Validation – Project Management

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  • Cleaning Validation – Workshop and Trainings

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  • Process Validation – Execution

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  • Process Validation – Project Management

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  • Process Validation – Workshop and Trainings

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  • Water Systems Validation (WFI, PW and Pure Steam) – Execution

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  • Water Systems Validation (WFI, PW and Pure Steam) – Project Management

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  • Water Systems Validation (WFI, PW and Pure Steam) – Workshop and Trainings

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  • Quality Leadership Development

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  • Medical Devices EU Registration – Implementation and Improvement

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  • Medical Devices EU Registration - Routine Support

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  • Nitrosamines: Compliance with requirements - Implementation and Improvement

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  • Nitrosamines: Compliance with requirements - Routine Support

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  • Safe use of AI tools in Quality: Data Security and Process Optimization

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  • Quality Leadership Development – Competency Development Program

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  • Medical Device EU Registration – Strategic Consultancy

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  • Medical Device EU Registration – Routine Support

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  • Nitrosamines – Strategic Consultancy

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  • Nitrosamines – Routine Support

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  • Quality Leadership Development – Competency Evaluation

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  • Quality Leadership Development – Development Plan Creation

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  • Medical Device EU Registration – Strategy Definition

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  • Medical Device EU Registration – Operational Documents Creation

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  • Medical Device EU Registration – GAP Assessment

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  • Medical Device EU Registration – Execution

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  • Medical Device EU Registration – Project Management

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  • Medical Device EU Registration – Workshop and Trainings

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  • Nitrosamines – Strategy Definition

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  • Nitrosamines – Data Management Strategy Creation

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  • Nitrosamines – Drug Product Risk Management Strategy Creation

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  • Nitrosamines – Drug Substance Risk Management Strategy Creation (for NDSRI)

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  • Nitrosamines – GAP Assessment regarding ICH M7

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  • Nitrosamines – Analytical Strategy Creation

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  • Nitrosamines – Data Management Activities Execution

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  • Nitrosamines – Risk Assessment Creation

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  • Nitrosamines – Workshop and Trainings

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  • Nitrosamines – Project Management

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  • Nitrosamines – QMS Life Cycle Integration

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Wir verbessern Ihre Leistungen 

Machen Ihnen Prozessabstimmungen, Konformität, Projektmanagement und Herausforderungen in Bezug auf den Zeitplan Sorgen? Bei Zamann wandeln wir Ihre Herausforderungen in praxisnahe Lösungen um.

Unsere Expertise in Qualitätsberatung, Digitalisierung, globalem Projektmanagement sowie Validierung und Qualifizierung steigert Ihre Effizienz, sichert die Einhaltung von regulatorischen Anforderungen und ebnet den Weg zum Erfolg.

Gemeinsam können wir Ihr Wachstum und Ihre Entwicklung in der Pharma und Life Sciences Branche beschleunigen. 

Professionals discussing about Quality Management System, representing Zamann's global project services

Globales Projekt Management Mehr erfahren 

Quality consultant analyzing data for compliance, representing Zamann's Quality Consultancy service.

Qualitätsberatung Mehr erfahren 

Group of professionals discussing digital transformation strategies, indicating Zamann's Digitalization services

Digitalisierung  Mehr erfahren 

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Validierung und Qualifizierung  Mehr erfahren 

Wie funktioniert eine Zusammenarbeit? 

Unsere Zusammenarbeit zielt darauf ab, Ihre individuellen Bedürfnisse zu verstehen und darauf einzugehen. 

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1. Terminanfrage

Sie beantragen über unsere Website eine kostenlose Erstberatung und beantworten einige Fragen zu Ihren Bedürfnissen

2. Einführungsgespräch  

Einer unserer Experten führt ein erstes Gespräch mit Ihnen, um Ihre Anforderungen zu verstehen und Ihnen den richtigen Spezialisten für Ihren Fall zuzuweisen.  

3. Experten Beratungssitzung

Ein Berater bietet 60 Minuten individuelle Beratung an, berücksichtigt Ihre spezifische Situation und entwickelt gemeinsam mit Ihnen eine Lösung für Ihre Herausforderung. 

4. Langfristige Partnerschaft  

Nach der Erstberatung besteht die Möglichkeit, dass wir Sie langfristig bei der Umsetzung Ihrer Qualitäts- und Unternehmenslösung begleiten.  

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Lassen Sie uns das gemeinsam angehen 

Mit uns erhalten Sie mehr als nur Dienstleistungen. Sie gewinnen einen engagierten Partner, der Sie konsequent unterstützt und Ihren Erfolg in der Pharma und Life Science Branche sicherstellt. 

Zamann arbeitet hauptsächlich mit den folgenden Sektoren zusammen

Life Science und Qualitätsmanagement ist unser Zuhause. Wir verwandeln Ihr Unternehmen in einen Qualitäts-Champion – dabei unterstützen wir Sie bei täglichen QMS und Projekt Aktivitäten, validieren und implementieren Softwarelösungen, entwickeln umweltfreundliche medizinische Geräte oder programmieren Software. Sie wählen, was Sie benötigen. 

Pharma, Biotech, Medizinprodukte und Tiergesundheit 

Zamann ist für praxisnahe und innovative GMP-Dienstleistungen bekannt. Als innovativer Akteur in der Branche bringen wir frischen Wind und eine neue Perspektive ein – sei es in Bezug auf schlanke Validierung, Prozesse oder Unternehmensstrukturen. 
Profitieren Sie von der neuen Compliance-Generation.  

Lebensmittel-, Chemie-, Kosmetik- und Nahrungsmittelindustrie 

Wir sind in der gesamten Pharma, Medizin und Nahrungsmittel Industrie tätig und beziehen auch Sie mit ein, wenn sie kosteneffiziente und sichere Prozesse lieben. Zamann ist nicht nur ein Dienstleister für Ihr Unternehmen, sondern auch eine Plattform zum Austausch bewährter Verfahren zwischen Industriegrößen und ermöglicht neue Geschäftsmöglichkeiten.   
Werden Sie noch heute ein Branchenführer  

Anbieter von Life-Science  

Sie sind ein Zulieferer für europäische Life-Science-Unternehmen oder möchten es werden? Möchten Sie eine schnelle und kosteneffiziente Markteinführung? Dann nehmen Sie Kontakt mit uns auf, um gemeinsam Ihre Go-to-Market-Strategie zu entwickeln und umzusetzen.  
Werden Sie ein Life-Science-Lieferant