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Ana Barranco

Decantum Systems S.L
Kits Toxicology

Contact Information:

C/Santiago Grisolía 2

Years in Business:



Clients I'm Seeking:


CLINICAL AND TOXICOLOGICAL SECTOR Clinical Analysis Labs Hospitals (Toxicological Department) Forensic Toxicology Labs Scientific Police Doping analysis (Sport controls) FOOD SAFETY SECTOR Public health Labs Agrofood Labs Animal health Labs Food analysis companies Food technology centers Institutes for Food Research

About My Business:


We commercialize a wide range of kits for ultrafast extraction of: 1.- Veterinary residues (B-Agonists, Steroids, Stilbenes, Corticoids, Benzodiazepines, Sulphonamides, Thyreostatics , Chloramphenicol) in biological matrices of animal origin (eye, urine, entrails, tissues, animal feed, honey) applied to food safety 2.- Abuse, Doping and psychiatric drugs (Anticonvulsants, Anticholinergics, Tetracyclic and Tricyclic antidepressants, Antiemetic and gastroprokinetic agents, Anthelminthics, NSAIDs, Antipsychotics, Antitussives, Antihistamines, Anxiolytic psychoactive, Benzodiazepines, Barbiturates, Fenotiazines, Neuroleptics, Narcotic analgesics, Psychostimulants, Local Anesthetics, Sedative-Hypnotics, Opiates, Anti-diabetics, Alpha-adrenergic Agonists , Anti-diarrheal drug, Anticholinergics, Beta-blockers and Hallucinogens) in human matrixes as urine, saliva, blood and entrails/tissues with application to toxicological control . These innovative reagent kits allow extracting the analytes in a very short time through liquid-liquid extractions and then they are detected and quantified by chromatographic equipment (GC-MS/MS or LC-MS/MS). These kits have the following advantages: - Allow extracting a wide range of different drugs in only one test. - Reduction the treatment time of sample. - Minimum number of lab equipment. - The residues to inject are free of interferences. - Easy, simple, cheap and effective techniques. - The kit contains all reagent ready to use. - Includes protocol and analysis certificate. - They comply with the LMRs according to Commission Regulation (UE) No 37/2010. - We have performed validations according to Guidance for Industry, Bioanalytical Method Validation (FDA, 2001).

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