Introduction
Addressing an Unmet Need
Product Info
Pharmacological class
Clinical Studies
Menopausal Symptoms
FemarelleŽ & Bone Loss
    . Effect on Bone Mineral Density
    . Mechanism of action in the bone
    . Skeletal tissue & the uterus
    . Histology of skeletal tissue
FemarelleŽ & Breast Tissue
FemarelleŽ as a SERM
FAQ
Manufacturing Procedure

   
Manufacturing Procedure

Femarelle® is manufactured according to state of the art industrial standards. The product is subjected to rigorous and comprehensive microbiological and biochemical testing throughout the manufacturing process. Its pharmacological efficacy and shelf life are constantly monitored, and state-of-the-art technology is used to maintain the long-term stability of the active ingredient.

Femarelle® is produced from a botanical source (non-genetically modified). No chemicals are used in the manufacturing process. The manufacturing procedure is carried out according to the strictest standards of quality control, and is certified by ISO 9001-2000, cGMP, and BVQI as well as the environmental ISO 14001.

Se-cure Pharmaceuticals Ltd. is committed to ensuring that each capsule produced is characterized by identical therapeutic features according to the accepted standards of the pharmaceutical industry.

 
Home   Site Map   Disclamer © Se-cure Pharmaceuticals Ltd.