Compliance seminars® 

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Key2Compliance® solves all your training needs in terms of regulatory requirements, GMP, GXP and quality systems. Knowledge of these requirements is an important key to developing, manufacturing and distributing safe and effective drugs and medical devices. Training from Key2Compliance® makes the knowledge easily accessible, applicable and makes it clear how the regulatory requirements affect your business.

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Cleaning validation of pharmaceutical process equipment

Copenhagen, Denmark
Cleanrooms and cleaning, Sterile products, Validation and Qualification

Auditor/Lead Auditor – Läkemedel och medicinteknik

Mar 13
- Mar 15, 2024
Stockholm, Sweden
Auditing/Inspection, Validation and Qualification

GMP Master Class

Apr 10
- Apr 11, 2024
Copenhagen, Denmark
QC-lab, Quality management and QA

Grundlæggende om GMP

May 2
Copenhagen, Denmark
General

Sterilization of Medical Devices

May 13
- May 17, 2024
Copenhagen, Denmark
Auditing/Inspection, Bioburden, ISO 11737, Sterilization, Validation

GMP for QC laboranter

May 16
QC-lab

Validering och kvalificering

May 21
- May 22, 2024
Stockholm, Sweden
Validation and Qualification

Medical Device Supplier Control and Outsourcing

May 28
- May 29, 2024
Copenhagen, Denmark
Quality management and QA

Design Controls for Medical Devices

May 29
- May 30, 2024
Copenhagen, Denmark
Design Control

GMP-krav på datoriserade system

Jun 11
- Jun 12, 2024
Stockholm, Sweden
Computers/Software

Strategic communication

Jun 12
- Jun 13, 2024
Copenhagen, Denmark
General, Quality management and QA

Requirements to place Medical Device Software and Health Software on the market

Jun 12
- Jun 13, 2024
Copenhagen, Denmark
Computers/Software

Auditor / Lead Auditor – Pharmaceuticals and Medical Devices

Jun 17
- Jun 19, 2024
Copenhagen, Denmark
Auditing/Inspection

Validation and qualification

Jun 18
- Jun 19, 2024
Copenhagen, Denmark
Validation and Qualification

Medical Device Quality Management Systems (QMS)

Jun 25
- Jun 27, 2024
Copenhagen, Denmark
Quality management and QA

Medical Device Product Life Cycle

Oct 8
- Oct 9, 2024
Stockholm, Sweden
Quality management and QA, Regulatory Affairs

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