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Manufacturing

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In the composition of Pierpaoli Products every detail has been studied in order to provide maximum benefit to the metabolic, endocrine and immunobiological system of those who take it.

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For example, the exclusive formulation of Melatonin Zinc-Selenium Pierpaoli has been developed 20 years ago in Switzerland, according to a very specific manufacturing method (the pharmaceutical procedure for the correct production of the Original Pierpaoli Formula of Melatonin Zinc-Selenium) which guarantees the precise therapeutic function of the Product, in accordance with Walter Pierpaoli’s scientific instructions, procedure which is scrupulously followed in each production manufacturing process.

 

The method and the manufacturing formula are reported in the registered manufacturing method that include detailed instructions for each stage of the manufacturing process (verification of materials, temperature, how and when carry out process checks, samples for carrying out analyzes, instructions on how to store loose products). 

 

For each lot the specific approved features of the raw materials, the packaging materials nd the sampling procedures are defined. There are specifications of criteria for approving raw materials and packaging materials as well as the modalities for releasing the finished product and the checks to be carried out during the manufacturing process. Each lot has its own processing report.

 

Obviously the production takes place in compliance with the regulations in force and applying the pharmaceutical method in the evaluation of dangers and risks and in the adoption of measures of control aimed to prevent the onset of hygiene and health problems. The quality of the finished product is ensured by guaranteeing ISO-assimilable and / or GMP processing procedures, so that the characteristics of the finished product correspond to what is required and do not undergo any alterations during processing.

 

For each lot, surveillance activities to protect the Integrity and Safety of the Finished Product are implemented, including, for example:

 

  • Analysis of the raw materials to verify the correspondence of possible titles of active principles and the absence of contaminants such as pathogenic bacteria, aflatoxins, heavy metals, pesticides, solvent residues, allergenic substance
  • Control of surfaces and backgrounds to verify the effectiveness of cleaning procedures and prevent cross-contamination problems
  • Implementation of automated line controls to avoid the risk of incomplete or partial product, completed by a constant and effective processing control activity operated by qualified Quality Control personnel, according to procedures acquired by the pharmaceutical field
  • Analytical checks on the Finished Product and issue of the product’s Certificate of Conformity for the marketing of the finished product.

 

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We produce supplements, pharmaceuticals and cosmetics, according to Dr. Walter Pierpaoli’s instructions.