Quality care


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PharmaPack devotes the greatest possible care to safeguarding the quality of your products. To achieve this we work with a thorough certified quality system.

Our Quality department monitors all quality  aspects within the entire packaging process.
Our Quality department monitors all quality
aspects within the packaging process.

Our quality policy is aimed at packaging and distributing your pharmaceutical products in such a way that they meet the most stringent quality requirements. We therefore take the greatest possible care of your batches from start to finish. Our personnel are properly trained and work with the most suitable equipment for warehousing and production tasks.
Our objectives are clear:

  • To provide you with the agreed quantity of products at the agreed time in accordance with the agreed specifications;
  • Providing a high quality at competitive prices.


Quality system

Our quality system complies with ISO 9001: 2008, the GMP/GDP guidelines of the EU, and national and international regulations and legislation. Our customers as well as certification and monitoring bodies regularly visit us for inspection purposes.

In order to guarantee quality down to the last detail, our working methods and rules are laid down in SOPs (Standard Operating Procedures). We assess the functioning of our organization on the basis of critical performance indicators. Furthermore, we devote plenty of time to staff training as well as continuous optimization of the entire packaging process.

PharmaPack works with the utmost suitable  machinery.
PharmaPack works with the utmost suitable
machinery.

Quality department

The Quality department consists of Quality Assurance employees (QA), Quality Control employees (QC) and a Manager QA/QP.

Our QC employees strictly monitor all quality aspects of the entire packaging process by conducting line-clearance and in-process checks. QA employees are responsible for the development, implementation and maintenance of the entire quality system. They also conduct internal (at PharmaPack premises) as well as external (supplier) audits. QAs are furthermore responsible for the coordination of change control, resolving of complaints as well as abnormalities and the observance of improvement actions. Our Qualified Person finally assesses all batches produced upon release for transport