Danske oversættelser af US GMP

• US 21 CFR 210, 211 og 11

   (Lægemidler og Elektroniske dokumenter/signaturer)

• US 21 CFR 820 og 11

   (Medicinskt udstyr og Elektroniske
    dokumenter/signaturer)

- Smidigt lommeformat
- Wirebinding til enkel håndtering.
- Originalteksten parallelt med oversættelsen

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New GMP board game
- Ideal for refresher training

The GMP board game that tests and improves your GMP compliance, knowledge, attitude and awareness!  

Now on stock.     

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Kursus for lægemidler

Kursus for medicinsk udstyr

Kursus for lægemidler og medicinsk udstyr

København , april - juni 2013

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GMP for QC laboranter (14.5)

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GMP for Management (6.6)

København, september - oktober 2013

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Grundlæggende om GMP -Good Manufacturing Practices (27.9)

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GMP Up-dates - What's cooking (21.10)

Pharmaceutical and Biopharmaceutical industry

Medical Device industry

Pharmaceutical and Medical Device industry

May 2013 Stockholm

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Cleaning Validation - Strategy, techniques and regulations

June 2013, Copenhagen

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Quality System Requirements & Industry Practice

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Process Validation Requirements and Industry Practice

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Contamination control in cleanrooms - GMP requirements and industrial practice (US and EU)

October 2013, Copenhagen

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Corrective and Preventive Action (CAPA) Requirements and Industry Practice

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Design Control Requirements and Industry Practice

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GMP Compliance for Quality Control and Laboratory Operation

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CGMP: Interpretation and Application

November 2013, Copenhagen

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Best Practices for Global Investigational Medicinal Product (IMP) Management

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Good Distribution Practice (GDP) - A Practical Approach

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From Training to Learning - Improving GMP Performance

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Introduction to Risk Assessment and Risk Management

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Good Engineering Practice - A Practical Approach for Engineers