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

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
General

Processvalidering – Medicintekniska produkter – Kurs

Vad innebär processvalidering för medicintekniska processer? Vilka tillverkningsprocesser måste valideras? Hur ska vi genomföra och hur ska vi dokumentera?
Apr 22
Online
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

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