lab-top

TENUIS has approximately 1000 sq. m. available, located at the 2nd floor of Noval Building in Koxhas – Maminas Durrës, including laboratory spaces and offices.

The area hosts the Microbiology Department and Physico – Chemical Department.These structures in the building offer state-of-the-art technological platforms, scientific equipment and support services in order to meet international standards for testing and quality control laboratories.

Each of these departments has a unique HVAC (heating ventilation and air conditioning) system. Also they are equipped with HEPA filters, based on negative overpressure to ensure the minimization of contamination from one section to another (cross-contamination).

Laboratory

Our laboratory offers:

• Food testing
• Water testing
• Air testing
• Ground analysis
• Analysis of Pharmaceuticals

Sample control/processing (log-in, results data-entry, reporting) is facilitated by our computer Laboratory Management System Cartesio which tracks the sample job (batch) and provides the lab with work log (due dates) to help ensure all the work is organized and processed in accordance with the client's needs.

Cartesio includes security controls to ensure that information is controlled (locked) once the data is been documented and entered by the Analyst.

Reports can be delivered in a variety of formats at the customer's choosing, including email,hard-copy or both.

Our Laboratory is unique and one of its special kind in Albania for its well developed, powerful tools that perform analytical method suitable for numerous applications.  HPLC MS/ MS Triple Quadrupole can be used for identification and quantification of residual pesticides in water system. In investigation and monitoring of the quality of natural and waste waters it can be used for identification and quantification of pesticides. We can mention as well ICPMS to detect the presence of toxic metals, also  GC-Headspace  that estimates Organic Volatile Impurities and Residual Solvents. Dissolution test is a key analytical test used for detecting physical changes in an active pharmaceutical ingredient (API) and in the formulated product etc.

TENUIS offers three broad approaches to pharmaceutical analysis:

       testing raw materials and intermediates

       testing finished pharmaceutical products,

       chemical identity tests.

Also TENUIS performs these pharmaceuticals analysis:

Purified Water System Validation [TOC & Micro]

TOC Analysis of water by TOC Analyzer.

  • Analysis of Drugs (API) and Intermediates as per Pharmacopoeia or in-house specifications:
  1. Identification by FTIR,
  2. Elemental Impurities by ICP-MS

iii. Trace Metal Analysis by ICP-MS

  1. Purity, Assay, Related Substances by HPLC and GC
  2. Organic Volatile Impurities and Residual Solvents estimation by GC-Headspace
  3. Potentiometric Titration (Aqueous, non Aqueous , Argentometric)

vii. Moisture content by Karl Fischer Titrator

viii. Melting Range

  • Analysis of Pharmaceutical Dosage Forms (Formulations) as per Pharmacopoeia
  1. Content of drugs by HPLC, UV, GC FID
  2. Dissolution Test

iii. Disintegration Test

Contact Info NUIS: L81904506I

Contact Info

NUIS: L81904506I

Address: Rr.Dytësore Maminas–Vorë

(Km 2, Durrës, Albania)

Tel: +355 57 58 4035

Mobile: +355 68 80 42 045

email: info@tenuis.al

Submission Forms

Use below forms for your tests

Pharmaceuticals

Noval Laboratory offers three broad approaches to pharmaceutical analysis:

       testing raw materials and intermediates

       testing finished pharmaceutical products,

       chemical identity tests.

Also Noval Laboratory performs these pharmaceuticals analysis:

Purified Water System Validation [TOC & Micro]

TOC Analysis of water by TOC Analyzer.

  • Analysis of Drugs (API) and Intermediates as per Pharmacopoeia or in-house specifications:
  1. Identification by FTIR,
  2. Elemental Impurities by ICP-MS

iii. Trace Metal Analysis by ICP-MS

  1. Purity, Assay, Related Substances by HPLC and GC
  2. Organic Volatile Impurities and Residual Solvents estimation by GC-Headspace
  3. Potentiometric Titration (Aqueous, non Aqueous , Argentometric)

vii. Moisture content by Karl Fischer Titrator

viii. Melting Range

  •  Analysis of Pharmaceutical Dosage Forms (Formulations) as per Pharmacopoeia
  1. Content of drugs by HPLC, UV, GC FID
  2. Dissolution Test

iii. Disintegration Test