Instructor

Maria Axelsson

Maria has 25 years of quality experience in Life Science Industry, working with Pharmaceuticals, Medical devices, IVDs, and also the food industry. As an experienced trainer and qualified lead auditor, she combines deep regulatory knowledge with practical insights to deliver engaging workshops and courses.

She provides trainings in several areas such as Auditing, Validation/Qualification, GMP Basic, Updates and MasterClass level, Quality System Requirements, Documentation practices, Deviations, Investigations, CAPA.

Maria is today co-founder and partner at Vera Clarity & Quality AB, a company offering trainings, auditing and consulting services within quality and sustainability for the Life Science industry.

Related courses to Maria Axelsson

Auditor / Lead Auditor Course – Pharmaceuticals and Medical Devices

This tailor made training gives you the tools and skills required as Auditor or Lead Auditor in the Pharmaceutical and Medical Device industry.

Nov 9

- Nov 11, 2026

Copenhagen, Denmark

Auditing/Inspection

Process validation – Medical Devices – Course

Gain increased knowledge about both the preparations required and the main parts that are included in process validation for medical devices.

Oct 22

Online

Validation, Validation and Qualification

GMP Up-dates – Course

Changes and updates within the GMP regulations in the EU, US as well as a presentation of trends in Warning Letters, 483 observations and Recalls.

Online

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GMP MasterClass course

Get a comprehensive review of GMP compliance requirements and tools to master application and interpretation of these requirements in pharmaceutical production.

Oct 7

- Oct 8, 2026

Copenhagen, Denmark

GMP, Pharmaceuticals, QC-lab, Quality management and QA

Auditor/Lead Auditor – Läkemedel och medicinteknik – Kurs

Denna specialanpassade utbildning ger dig de verktyg och färdigheter som krävs som Auditor eller Lead auditor inom läkemedels- och medicinteknisk industri.

Auditing/Inspection, Validation and Qualification

Kvalitetssystemkrav för Medicinteknik

Förstå de centrala krav som måste vara uppfyllda för att utforma och förvalta ett kvalitetsledningssystem enligt regelverken i EU och USA.

General, Quality management and QA