The certified filter bag solution
SEFAR PHARMA GMP Bags is the certified filter bag solution for the pharmaceutical and nutraceutical industry. The design has been developed to avoid possible contamination from staple fibers coming from the needle felt.
An ePTFE microporous membrane laminated on the polyester or PTFE needle felt results in a high filtration efficiency. The high-conductivity stainless steel matrix incorporated in the antistatic version provides excellent protection against explosion (acc. ATEX).
The manufacturing process of the SEFAR PHARMA GMP Bags is compliant with EU 2023/2006 GMP. All the materials used conform to both EU 10/2011 and FDA CFR’s.
This means that the ready-to-use complete SEFAR PHARMA GMP Bags are the only filter bags existing in the market complying with EU 1935/2004.
SEFAR PHARMA GMP Bags are tailor-made, in accordance to the specific dimension and manufacturing detail required by the equipment.
Examples of the most common manufacturing solutions:
Tailor-made top connections (snap ring, steel ring etc.) available according to customer's design
Sefar filter solutions for OEM
Our products meet the specific needs of these filtration applications and are successfully running all over the world on all known GMP PHARMA Bag brands and OEMs, such as:
psl (Powder Systems Limited)
Filter media technology
Our customers can choose from a wide range of felt qualities required in the life science industry. These felts can be used for every type of filter sleeves, filter socks, dust bags and tubes.
Specially made for life science industries
Sefar controls every crucial production step from yarn production to the ready-to-use filters making possible a complete traceability of all critical parts.
Our unique market position in life science enables us to supply products to our customers that meet all required quality levels and compliances.
Sefar has perfected its manufacturing processes to meet the needs of the pharmaceutical industry. Our exclusive GMP compliant filter products are manufactured in our cleanroom following strict GMP guidelines.
GMP EC 2023/2006 or cGMP
FDA CFR 177
ATEX (Directive 2014/34/EU)