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TDM I – Neuroleptics – Serum

For quality monitoring of
Medidrug® TDMA series S-plus
quantitative measurements
Lyophilized serum-based reference material for accuracy monitoring of neuroleptics de- by chromatographic methods
termination. The indicated reference values are established within the bounds of proficien- cy testing “Therapeutic Drug Monitoring in Serum” by the GTFCh (Society of Toxicological and Forensic Chemistry). The direction of the proficiency testing association approved the These reference materials are produced on the basis of human matrices. The highly ac- Medidrug® TDMC series S-plus
curate manufacturing occurs in a very gentle Lyophilized serum-based reference material for accuracy monitoring of neuroleptics de- way. Analytical matrix effects are almost ex- termination. The indicated reference values are established within the bounds of proficien- cluded. We achieve this by granting a maxi- cy testing “Therapeutic Drug Monitoring in Serum” by the GTFCh (Society of Toxicological mal conformity of the products’ matrix with and Forensic Chemistry). The direction of the proficiency testing association approved the Therapeutic
Drug Monitoring
TDMA Serie S-plus
TDMC Serie S-plus
Component
Order information
* Sertinole and Zotepine: only for precision control LOT The catalogue code (REF) of products marked with this symbol defines a singular lot (batch) which has been produced especially for an external quality con-
trol (proficiency testing) organized by associations such as the GTFCh and the SFTA. After expiry of the validity or after being sold out this product is no longer available. New lots with similar compositions of components will be offered with a different catalog code. If the material has been approved by the direction of proficiency testing according to the organizing association or reference institution and thus get an internal quality control we proceed in this Get your update: Use our free newsletter and subscribe to
The provided mixture of the controls and their respective analyte concentrations are for overview purposes Contact us:
only and may differ from the current available batches. For the internal quality control, only the designated specification of the respective batch of the information leaflet is valid. Certified quality management according to DIN EN ISO 9001:2008 TDM II – Antidepressants – Serum

For quality monitoring of quantitative measurements by
Medidrug® TDMD series S-plus
chromatographic methods
Lyophilized serum-based reference material for accuracy monitoring of These reference materials are produced on the basis of human antidepressants determinations in serum. The indicated reference matrices. The highly accurate manufacturing occurs in a very values are established within the bounds of proficiency testing “Thera- gentle way. Analytical matrix effects are almost excluded. We peutic Drug Monitoring in Serum” by the GTFCh (Society of Toxicologi- achieve this by granting a maximal conformity of the products’ cal and Forensic Chemistry). The direction of the proficiency testing matrix with the matrix of the patients’ sample. Therapeutic
Drug Monitoring
TDMD series S-plus
Component
Order information
LOT The catalogue code (REF) of products marked with this symbol defines a singular lot (batch) which has been produced especially for an external quality con-
trol (proficiency testing) organized by associations such as the GTFCh and the SFTA. After expiry of the validity or after being sold out this product is no longer available. New lots with similar compositions of components will be offered with a different catalog code. If the material has been approved by the direction of proficiency testing according to the organizing association or reference institution and thus get an internal quality control we proceed in this Get your update: Use our free newsletter and subscribe to
The provided mixture of the controls and their respective analyte concentrations are for overview purposes Contact us:
only and may differ from the current available batches. For the internal quality control, only the designated specification of the respective batch of the information leaflet is valid. Certified quality management according to DIN EN ISO 9001:2008 1.16 TDM I – NeurolepticsSerum
1.17 TDM II – AntidepressantsSerum
 Product / price available on request Product available only as long as still on stock – will be cancelled
LOT Product has been produced especially for an external quality control (proficiency testing). The catalogue code REF refers to a singular lot
(batch). After expiry of the validity or being sold out it is no longer available. If possible new lots with similar compositions of components will be offered with a different catalogue code. Company & products
Since 25 years MEDICHEM stands for the development and production of in-vitro-diagnostic products at highest level.
More products from our extensive range of reference materials:  Alcohols: ethanol, methanol, congener alcohols  Alcohol biomarkers: EtG, EtG-D5, EtS, FAEE  Therapeutic drugs and drugs of abuse: Complete product overview including prices on the web: Please do not hesitate to contact us if you have any further questions.

Source: http://www.medichem.de/PDF/TDM_E.pdf

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