The production process

We collect plasma and transform it into lifesaving plasma-derived therapies.

Each plasma-derived therapy we create is controlled, fractionated, purified, virus inactivated and inspected before being used to change and save the lives of millions of patients worldwide.

Plasma-based therapies treat rare, genetic and chronic diseases such as hemophilia and immune deficiency disorders. They are also used for trauma and burn victims and for critical care procedures including major surgeries, cancer treatments and organ transplants.



The donor’s identity is verified; details are managed in our donor registry system.

Donors must be: +18 years old, +50kg in weight and healthy.


Each donor completes a health questionnaire and physical screening.


The donation process takes 45 to 90 minutes. From 300 to 880ml of plasma is taken each time.


Donations are labelled with a barcode so at any point in the process the donor can be traced.


The plasma is tested for viruses like hepatitis, HIV and parvo virus B19.


Visual inspection

As a first step, individual plasma donations are visually inspected.


After the visual inspection, each donation is barcode scanned and all plasma codes are entered into the Octapharma production data system.


Donations are stored in a freezer at -25°C.

Controlling the plasma that enters production

Single donation control (SDC) is the foundation of traceability of all of our individual plasma donations. Learn about the process from Annabelle, who works at our Lingolsheim site (France). 


Processing plasma

Biochemical processes to separate plasma into its various components to gain the desired proteins for Octapharma products.

Separating plasma proteins

Fractionation is the separation of plasma proteins by influencing their solubility, by changing the ethanol concentration, pH-value and temperature. Different proteins are extracted under varying conditions. Knuth Litke, Fractionation Manager, Springe (Germany) explains more in his video.


Purification processes

Different processes are used to filter out potential contaminants and pathogens:

  • Precipitation

  • Ultra/diafiltration

  • Chromatography

Virus removal

To remove or inactivate viruses the following processes are used:

  • Solvent detergent

  • Nanofiltration

Purifying products

While purifying our products during a night shift at our site in Stockholm (Sweden), Process Operator Thomas explains the process:

In fine fractionation, we take the intermediates we receive from basic fractionation and purify them into final products.

Learn how intermediates are purified and transformed into products by watching his video.


The filling process

Octapharma has an aggressive modernization plan that ensures continual investment in new state-of-the-art filling lines for our production sites. Fully automated lines increase filling capacity, which means reliable supplies of products for our patients. Sara, Inter-site Team Member, in Stockholm (Sweden) explains in this video how technology in the filling process can improve the safety of our products.


Visual inspection

The finished product is inspected for potential contamination and damage and released for packaging based on country specific requirements.


Products are packaged as per country requirements and stored in modern temperature controlled warehouses until they reach their final destination.



Each batch of all final products is tested for compliance to specified standards to ensure patient safety.


100% review of all  process parameters.

Internal release

Compliance with all requirements leads to internal release of the batch.


Samples of every plasmapool are tested again for absence of viral markers as well as for virus DNA/RNA.

External testing

Batches are also tested externally and released by an Official Medicine Control Laboratory (OMCL).

External control

To release the batch of final product, an external control of all defined criteria is required. After this, the medicines can be used by patients.

Performing analytical methods to test quality

Performing analytical methods to test quality is the main task of the Quality Control Analytics department. “Everyday, we test the final containers, intermediates, in-process samples and stability samples” says Bernhard, Senior Technician, at our Vienna site (Austria).

Learn how this is done by watching his story.


Providing life saving treatments

Patients all around the world rely on our products to live a normal life.

  • 1,000,000+ people worldwide are living with bleeding disorders such as hemophilia.

  • 300+ immune diseases are treated with our products.

  • 1,200 plasma donations are needed to treat one severe hemophilia A adult patient with FVIII prophylaxis for one year.