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Quality Assurance
(medical devices, pharmaceuticals, combination products and raw materials)
Qmed Consulting ApS supports you in building up, improving and/or maintaining quality assurance systems based on GMP, ISO 13485 and ISO 9001.
We have extensive knowledge and experience in all aspects related to quality assurance e.g.:
• Preparing quality manuals, procedures and instructions
• Document management
• Building up and checking of batch records and log books
• Rules for quality documentation
• Handling of non-conformities and complaints
• Release of raw materials, bulk and finished products
• Assisting you during audits from authorities or customers
• Assisting you in performing your own internal or external audits
• Training staff in quality issues and quality documentation
All services can be provided as stand alone or full package.
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