GMP Training Courses - Barcelona

Quality Risk Management

Barcelona, Spain

16/17 September 2026

Quality Risk Management An ICH Q9 Training Course

Validation of Analytical Test Procedures & Measurement Uncertainty

Barcelona, Spain

13-15 October 2026

Validation of Analytical Test Procedures & Measurement Uncertainty

Setting Specifications AND Stability Testing

Barcelona, Spain

3-5 November 2026

Setting Specifications AND Stability Testing

Setting Specifications and Acceptance Criteria

Barcelona, Spain

3/4 November 2026

Setting Specifications and Acceptance Criteria

Stability Testing for Drug Substances and Drug Products

Barcelona, Spain

4/5 November 2026

Stability Testing for Drug Substances and Drug Products With Updates on the new ICH Q1 Guideline!

Europe's biggest Qualified Person Conference - 21st QP Forum

Barcelona, Spain

26/27 November 2026

Europe's biggest Qualified Person Conference - 21st QP Forum With Pre-Conference Sessions on 25 November 2026

Qualified Person Education Course Module A & IMP Pre-Course Session

Barcelona, Spain

9-11 March 2027

Qualified Person Education Course Module A & IMP Pre-Course Session Understand the Implications of becoming a QP

GMP/FDA Compliance in Analytical Laboratories

Barcelona, Spain

9-11 March 2027

GMP/FDA Compliance in Analytical Laboratories How to implement cGMP requirements in the everyday practice of quality control laboratories

Pre-course Session: Investigational Medicinal Products (IMP) QP Education Course

Barcelona, Spain

9 March 2027

Pre-course Session: Investigational Medicinal Products (IMP) QP Education Course

Qualified Person Education Course Module A

Barcelona, Spain

10/11 March 2027

Qualified Person Education Course Module A Understand the Implications of becoming a QP

The Validation Manager in the Pharmaceutical Industry

Barcelona, Spain

7-9 April 2027

The Validation Manager in the Pharmaceutical Industry

The GMP-Auditor

Barcelona, Spain

13-15 April 2027

The GMP-Auditor Initial and Continuous Professional Training for GMP Auditors