About QACS Ltd.

To provide Pharmaceutical analysis for quality control, design, research and development of pharmaceutical proprietary medicines QACS is GMP certified and it’s methodologies stay in accordance with EDQM & FDA. Equipped with Microbiological, Chemical and Molecular premises, the Lab provides 

-Challenge testing e.g. preservation efficacy to assess adequacy against microbial contamination -Pharmaceutical Stability testing to determine storage conditions and shelf life
-Extractables & Leachables studies  

Our GMP compliant lab also develop and implement validation protocols to document method suitability. Pharma validation services include Method validation and Transfer method Environmental monitoring.

Environmental monitoring & microbial Identification services are provided via DNA testing as well as microbiologically. Pharma testing services involve Nitrosamine testing, Medical device testing and others.

  • GR
  • 2016
    On CPhI since
  • 100 - 249
Contract Service
Contact info

Products from QACS Ltd.

  • Challenge Testing for Pharmaceutical

    Product Challenge Testing for Pharmaceutical

    QACS, The Challenge Test Laboratory, we conduct pharmaceutical challenge testing e.g. Antimicrobial Effectiveness Testing to substantiate preservation adequacy against microbial contamination which may occur under reasonably foreseeable conditions of storage and use. The Lab is GMP certified for microbiological testing (non-sterility) of human and veterinary medicinal products in various dosage forms. [email protected]

  • Method Development & Method Validation

    Product Method Development & Method Validation

    QACS Labs perform pharmaceutical testing services during and after drug development in order to ensure GMP compliance and product safety. 

    Method validation studies aim to demonstrate analytical suitability of procedures according to their intended use/purpose. Transfer method protocols ensure, that results generated by sending and receiving laboratories are equivalent with predetermined acceptance criteria. The equipment available for the development and the validation of analytical methods is UPLC-MS/MS, HPLCs, GC-MS, GC-HS-MS, ICP-MS, AAS, IC.

    Contact [email protected]

  • Cleaning Validation

    Product Cleaning Validation

    High-performance liquid chromatography (HPLC) is used to ensure that a routine cleaning process performed on manufacturing equipment removes all residues of previously manufactured products. In HPLC assay verification, we validate linearity, intermediate precision, recovery and specificity. Cleaning validation for manufacturing equipment includes testing of preparations & storage of tanks, filling nozzles and instruments.

    QACS Labs develop and implement microbiological method validation protocols, to document method suitability.[email protected]

  • Elemental Impurities Testing

    Product Elemental Impurities Testing

    QACS Ltd, provides elemental impurities testing and risk assessment studies using ICP-MS and AAS technology.

  • Extractables & Leachables studies

    Product Extractables & Leachables studies

    We test for organic and inorganic components, Volatile, Nonvolatile residues and Elemental impurities. E/L studies are performed with High-performance liquid chromatography (HPLC) Gas chromatography mass spectrometry (GC-MS) Liquid chromatography mass spectrometry (LC-MS) Inductively coupled plasma mass spectrometry (ICP-MS) Ultraviolet-visible spectroscopy (UV-VIS) Packaging Compatibility studies are also provided. Contact [email protected]

  • Molecular Pharmaceutical Testing

    Product Molecular Pharmaceutical Testing

    QACS Lab uses molecular technology to provide pharmaceutical testing services in rapid turn around times. DNA Microlab, member of QACS assists pharmaceutical manufacturing and monitoring processes in order to secure the absence of microbial contamination via Microbial Species Identification of Microbial Contaminants & Pathogen detection  testing services. For laboratory testing solutions, our highly engaged team of scientists will provide all the necessary information based on your product needs at [email protected]

  • Nitrosamine Impurity Testing

    Product Nitrosamine Impurity Testing

    QACS Ltd offers nitrosamine impurity testing and method validation for sartans, ranitidine, pioglitazone, esomeprazole and other pharmaceutical products. Implementation of EDQM guidelines by GC-MS and UHPLC-APCI-MS/MS. QACS  GMP compliant methodologies stay in accordance with EDQM & FDA. We test final, recovered, raw, packaging, cross-contaminated materials, API’s & Waters.Contact [email protected]
  • Stability studies & Storage

    Product Stability studies & Storage

    QACS provides pharma stability services based on international standards and custom solutions. We test API’s, raw materials and final products in recommended environmental storage conditions such as Temperature, Humidity, Light and Duration-Long term/Accelerated.

    Our GMP certified laboratory system allows for pharmaceutical quality evaluation at specific time intervals and under controlled and monitored conditions. Pharmaceutical stability studies are supported by walk-in chambers, thermal stability chambers, humidity control climatic chambers and storage space.

    Contact [email protected]

QACS Ltd. Resources