Overview
For a person to be named on a Manufacturing Importation Authorisation (MIA) as a Qualified Person (QP), s/he must be approved by the Competent Authority issuing that MIA as being eligible to be named as a QP. The Competent Authority must be satisfied that Directive 2001/83/EC (Article 49) requirements as transposed into the national legislation (Medicines Act 2003 Article 38 (1e) and Regulation 9 of L.N. 381 of 2005 as amended) are fully met.
What you'll get
Any person who wishes to be eligible as a 'Qualified Person' (QP) with the Medicines Authority in Malta.
Eligibility
Applications are being considered as being positively assessed and hence eligible for a QP interview if a number of criteria are met, particularly EU citizenship or permanent Maltese residence with working permit; work experience in the quality aspect of an EU/EEA/MRA Competent Authority authorised manufacturing facility producing medicinal products for human use and covering the dosage form/s for which s/he will be interviewed; a primary degree in a scientific discipline.
How to apply
Fill in the online form, print it, sign it and send to:
The Medicines Authority
The Malta Life Sciences Park
Sir Temi Zammit Buildings
San Ġwann SGN 3000
Interviews are usually carried out twice a year, one interview session generally held in the first quarter and another session held in the last quarter of every calendar year (subject to availability of applications eligible for interview).
The Medicines Authority
The Malta Life Sciences Park
Sir Temi Zammit Buildings
San Ġwann SGN 3000
Interviews are usually carried out twice a year, one interview session generally held in the first quarter and another session held in the last quarter of every calendar year (subject to availability of applications eligible for interview).
Timeline
Submission of Application
Vetting of Application
10 days
Approval of Application
6 months
Delivery of Service
6 months