Training – Manufacturing Authorisation (MIA) Responsibilities and Oversight
Manufacturing Authorisation training.
2 000 Skr
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Purpose:
This training package provides structured awareness of the regulatory, quality, and operational responsibilities associated with holding and maintaining a Manufacturing Authorisation (MIA).
Regulatory Alignment:
EU GMP requirements and national authority expectations applicable to Manufacturing Authorisation holders. This training supports awareness and competence but does not replace governing SOPs, validation activities, or licence conditions.
Included Files:
• Editable MIA-focused training slide deck(s)
• Facilitator notes and discussion points
Format:
Microsoft PowerPoint (fully editable)
Intended Users:
Pharmaceutical manufacturers, marketing authorisation holders, Qualified Persons, production management, and quality assurance teams involved in MIA oversight and compliance.