HyClone* Calf Serum, EMEA Conforming (U.S.), Iron-Supplemented

The European Agency for the Evaluation of Medicinal Products (EMEA) has issued two directives that apply to the use of bovine serum in the production of medicinal products.

• EMEA/CVMP/743/00-FINAL from the Committee for VeterinaryMedicinal Products (CVMP) Guideline on Requirements and Controls Applied to Bovine Serum Used in the Production of Immunological VeterinaryMedicinal Products
• EMEA/CPMP/BWP/1793/02 from the Committee for ProprietaryMedicinal Products (CPMP) Note for Guidance on the Use of Bovine Serum in the Manufacture of Human Biological Medicinal Products

To support medicinal manufacturers who utilize bovine serum in their processes, a line of EMEA conforming products that meet the scope of both directives has been created.

We recognize the need for high quality, traceable bovine serum, which is tested (and inactivated as required) to meet both directives.Where applicable, our EMEA Conforming products are tested per European Pharmacopoeia protocols and irradiated at the required minimum dose. These EMEA Conforming products provide medicinal manufacturers with the assurance of receiving high quality, consistent product that conforms to the requirements. Complete versions of both

directives can be found atwww.emea.eu.int.

Iron-Supplemented Bovine Calf Serum is collected by venipuncture from formula-fed veal calves (16 - 22 weeks at time of collection), which produce exceptionally high levels of transferrin.We carefully supplement this serum with iron to load serum transferrin levels to physiological levels. After supplementation, our Iron-Supplemented Bovine Calf Serum contains three to four times as much available iron and transferrin as FBS or equine serum.Many researchers have found this product to be an excellent and cost-effective alternative to FBS. Growth promotion studies have demonstrated many applications for Iron-Supplemented Bovine Calf Serum and show how it often outperforms FBS in many applications. As with all our calf serum products, this product is sterile filteredusing three sequential 100 nm (0.1 µm) pore-size rated filters.

Hemoglobin (spectrophotometric): ≤10 mg/dl

Sterility Testing(Current USP and EP Ph.Eur. 2.6.1) Bacteria & Fungi: No Growth

Fluorescent Antibody

Bluetongue: Not Detected

Bovine Adenovirus: Not Detected

Bovine Parvovirus: Not Detected

Bovine Respiratory Syncytial Virus: Not Detected

Bovine Viral Diarrhea Virus: Not Detected

Bovine Leukemia Virus: Not Detected

Rabies: Not Detected

Reovirus: Not Detected

Cytopathogenic Agents, e.g. IBR: Not Detected

Hemadsorbing Agents, e.g. PI3: Not Detected

(Points to Consider and EP Ph. Eur. 2.6.7)

Large Volume, Direct Culture: Not Detected

Hoechst DNA Stain: Not Detected

Ouchterlony/Double Immunodiffusion: Satisfactory

Antibodies: Pass

Interference/Comparative Titration: No Interference

Quantitation: Tested

Gamma Irradiation >30kGy (>30Mrad)

Bovine Viral Diarrhea Virus: Not Detected

Antibodies: Pass

Interference/Comparative Titration: No Interference

Quantitation: Not Detected

Certificate of Suitability: Included