Quality Control (QC) Testing Services

With expertise in custom synthesis, analytical services, and drug development.
We are here to support all your research needs by reducing the project timeline and cost.

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Our Partners:

ARSI Canada
Identity Testing

We conduct identity testing to confirm the identity of drug substances and products using techniques such as chromatography (HPLC, UPLC, GC), spectroscopy (UV-Vis, IR), and mass spectrometry (LC-MS/MS, GC-MS).

ARSI Canada
Purity Testing

For the detection and quantification of proteins, antibodies, and biomarkers. Our purity testing services assess the purity of drug substances and products, including content uniformity, related substances, and residual solvents, using validated analytical methods and regulatory-compliant protocols.

ARSI Canada
Potency Testing

We perform potency testing to determine the concentration or activity of active pharmaceutical ingredients (APIs) in drug formulations using validated assays, bioassays, and pharmacopoeial methods.

ARSI Canada
Dissolution Testing

Our dissolution testing evaluates the rate and extent of drug release from solid dosage forms using automated dissolution apparatus, ensuring consistent and reproducible drug release profiles.

ARSI Canada
Microbiological Testing

We offer microbiological testing services to assess the microbial quality of pharmaceutical products, including sterility testing, microbial enumeration, and microbial identification, following pharmacopoeial methods and regulatory guidelines.

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Why ARSI Canada Inc.?

Choosing ARSI Canada Inc. for your quality control (QC) testing needs means partnering with a team dedicated to ensuring the quality, safety, and efficacy of your pharmaceutical products. Our state-of-the-art facilities, experienced scientists, regulatory expertise, and commitment to timely and reliable results make us a trusted partner for QC testing.

Get in touch with ARSI Canada Inc. for comprehensive QC testing services and ensure the quality and safety of your pharmaceutical products with confidence.

FAQs about Quality Control (QC) Testing at ARSI Canada Inc.

What is quality control (QC) testing in pharmaceutical manufacturing?

Quality control (QC) testing in pharmaceutical manufacturing involves evaluating the identity, purity, potency, and performance of drug substances and products to ensure their quality, safety, and efficacy.

Why is QC testing important in pharmaceutical manufacturing?

QC testing is important in pharmaceutical manufacturing to ensure product safety, regulatory compliance, batch release, and customer confidence. It verifies that pharmaceutical products meet established quality standards and regulatory requirements.

What types of QC tests does ARSI offer?

ARSI offers a wide range of QC tests, including identity testing, purity testing, potency testing, dissolution testing, and microbiological testing, to assess the quality and performance of pharmaceutical products.

How does ARSI ensure the accuracy and reliability of QC test results?

ARSI ensures the accuracy and reliability of QC test results through state-of-the-art facilities, experienced scientists, validated analytical methods, regulatory expertise, and adherence to good laboratory practices (GLP) and good manufacturing practices (GMP).

Can ARSI customize QC testing protocols to meet specific project needs?

Yes, ARSI can customize QC testing protocols to meet the specific needs of each client and project. Our team works closely with clients to develop tailored testing strategies and protocols to ensure comprehensive quality assessment.

How long does QC testing typically take?

The duration of QC testing depends on factors such as the complexity of the test, sample size, and specific project requirements. Typically, QC testing can take anywhere from a few days to several weeks to complete.

What regulatory standards does ARSI comply with for QC testing?

ARSI complies with global regulatory standards, including guidelines set by agencies such as the FDA, Health Canada, and the European Medicines Agency (EMA). Our QC testing services meet the highest standards of quality, compliance, and regulatory scrutiny.

What documentation is provided after QC testing?

After QC testing, ARSI provides comprehensive documentation, including test reports, certificates of analysis, method validation reports, and regulatory submission documents. This documentation supports batch release, regulatory submissions, and quality assurance processes.

Can ARSI perform stability testing as part of QC testing?

Yes, ARSI can perform stability testing as part of QC testing to assess the long-term stability and shelf-life of pharmaceutical products. Our stability testing services evaluate product quality over time under various storage conditions.

How can I access ARSI's QC testing services?

You can access ARSI's QC testing services by contacting us through our website or directly via phone or email. Our team will work with you to discuss your QC testing needs and provide tailored solutions to meet your quality assurance requirements.

What types of pharmaceutical products can undergo QC testing at ARSI?

ARSI offers QC testing services for a wide range of pharmaceutical products, including solid dosage forms, liquid formulations, parenteral products, topical formulations, and inhalation products. Our expertise covers diverse product categories and dosage forms.

How does ARSI ensure confidentiality and data security for QC testing?

ARSI prioritizes confidentiality and data security for all QC testing projects. We have strict protocols in place to protect client information and ensure compliance with data privacy regulations, maintaining the highest standards of confidentiality and integrity.

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