Introduction to Method Development

At ARSI Canada Inc., we specialize in providing comprehensive method development services
tailored to the pharmaceutical and biotechnology industries. Our state-of-the-art facilities and
expert team ensure that every analytical method we develop is robust, reliable, and compliant
with regulatory standards.

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Importance of Method Development

Whether you are in the early stages of drug discovery or advancing through the development process, our method development services provide the foundation for accurate and consistent results. Method development is a critical component of the drug development process. Accurate and reliable analytical methods are essential for:

  • Ensuring Quality Control: Consistent product quality and safety.
  • Regulatory Compliance: Meeting stringent regulatory requirements.
  • Optimizing Formulations: Enhancing drug efficacy and stability.
  • Accelerating Time-to-Market: Streamlining the development process for quicker
    market entry.

Customized Chromatographic Methods

ARSI Canada
HPLC Method Development

High-Performance Liquid Chromatography (HPLC) is vital for accurate analysis. Our HPLC method development services include:

  • Quantification of APIs: Accurate measurement of active pharmaceutical ingredients (APIs) in various formulations.
  • Impurity Profiling: Identification and quantification of impurities anddegradation products to ensure product safety and efficacy.
  • Dissolution Testing: Custom HPLC methods for evaluating the release profiles of solid oral dosage forms.
ARSI Canada
GC Method Development

Gas Chromatography (GC) is crucial for analyzing volatile compounds. Our GC method development services include:

  • Residual Solvent Analysis: Detection and quantification of residual solvents in pharmaceuticals.
  • Volatile Organic Compounds (VOCs): Analysis of VOCs in
    environmental samples, food products, and packaging materials.
  • Flavor and Fragrance Analysis: Profiling flavors and fragrances in food and cosmetic products.

Spectroscopic Method Development

ARSI Canada
NMR Spectroscopy

Nuclear Magnetic Resonance (NMR) spectroscopy is essential for detailed structural analysis. Our NMR method development services include:

  • Structural Elucidation: Detailed molecular structure analysis of APIs and excipients.
  • Polymorph Identification: Identifying and characterizing different polymorphic forms of drug substances.
ARSI Canada
UV-Vis Spectroscopy

UV-Visible (UV-Vis) spectroscopy is used for concentration and purity assessments. Our UV-Vis method development services include:

  • Concentration and Purity: Determining the concentration and purity of proteins, nucleic acids, and other biologics.
  • Antioxidant Capacity: Evaluating the antioxidant capacity of food supplements and nutraceuticals.
ARSI Canada
LC-MS/MS Method Development

Liquid Chromatography-Mass Spectrometry (LC-MS/MS) combines separation and detection for complex analyses. Our LC-MS/MS method development services include:

  • Pharmacokinetic Studies: Quantifying drugs and metabolites in biological matrices.
  • Biomarker Analysis: Identifying and quantifying biomarkers in clinical research.
  • Impurity Detection: Detecting and quantifying impurities and
    degradation products.
ARSI Canada
GC-MS Method Development

Gas Chromatography-Mass Spectrometry (GC-MS) is ideal for volatile and semi-volatile compounds. Our GC-MS method development services include:

  • Environmental Analysis: Analyzing pollutants and contaminants in environmental samples.
  • Food Safety: Detecting pesticides, herbicides, and contaminants in food products.
  • Forensic Analysis: Identifying and quantifying drugs of abuse and toxic substances.

Formulation related method developments

ARSI Canada
Particle Size Distribution

  • Laser Diffraction Analysis: Methods for analyzing particle size distribution in powders, granules, and emulsions.
  • Dynamic Light Scattering (DLS): Size distribution of nanoparticles and colloids in liquid formulations.
ARSI Canada
Polymorph Characterization

  • X-ray Powder Diffraction (XRPD): Identifying and quantifying polymorphic forms of APIs.
  • Differential Scanning Calorimetry (DSC): Analyzing thermal properties of different polymorphs and excipients.
Contract research organization

Why ARSI Canada Inc.?

At ARSI Canada Inc., we are committed to delivering excellence in method development. Our experienced scientists, cutting-edge analytical technologies, and client-focused approach ensure that we provide the highest quality solutions for your drug development needs. Partner
with us for robust, reliable, and regulatory-compliant analytical methods.

Contact ARSI Canada Inc. today to learn more about our method development services and how we can support your drug development projects with precision and expertise.

Call us today for a free customized quote.

FAQs about Method Development at ARSI Canada Inc.

What is method development in pharmaceuticals?

Method development in pharmaceuticals involves creating and optimizing analytical methods to accurately measure the properties and concentration of drug substances and products. This process ensures the reliability, precision, and accuracy of analytical results, crucial for quality control, regulatory compliance, and successful drug development.

Why is method development important in drug development?

Method development is essential in drug development because it ensures that analytical methods are reliable and capable of accurately measuring the active ingredients, impurities, anddegradation products. This is vital for ensuring the safety, efficacy, and quality of pharmaceutical products, and for meeting regulatory requirements.

What types of method development services does ARSI Canada Inc. offer?

ARSI Canada Inc. offers a wide range of method development services, including HPLC method development, GC method development, NMR spectroscopy, UV-Vis spectroscopy, LC-MS/MS method development, and GC-MS method development. Our services are tailored to meet the specific needs of each clients project.

How does ARSI ensure the reliability of developed methods?

ARSI ensures the reliability of developed methods through rigorous validation processes. We follow International Council for Harmonisation (ICH) guidelines to validate methods for accuracy, precision, specificity, sensitivity, linearity, range, robustness, and reproducibility. This ensures that our methods are reliable and compliant with regulatory standards.

Can ARSI develop methods for complex formulations?

Yes, ARSI has extensive experience in developing methods for complex formulations. This includes particle size distribution, polymorph characterization, dissolution testing, stability studies, and rheological properties. We use advanced analytical techniques to address the unique challenges of complex formulations.

What is the process for developing a new analytical method at ARSI?

The process for developing a new analytical method at ARSI involves several key steps: understanding the clients needs, selecting appropriate analytical techniques, optimizing method parameters, conducting preliminary tests, validating the method according to regulatory guidelines, and providing comprehensive documentation and support.

How long does method development typically take?

The duration of method development varies depending on the complexity of the project and specific requirements. Typically, method development can take anywhere from a few weeks to several months. ARSI works closely with clients to provide accurate timelines and ensure timely delivery of results.

What industries benefit from ARSI's method development services?

ARSI's method development services benefit a wide range of industries, including pharmaceuticals, biotechnology, environmental testing, food and beverage, cosmetics, and forensics. Our expertise and advanced analytical capabilities make us a trusted partner for various sectors requiring precise and reliable analytical methods.

How does ARSI ensure regulatory compliance in method development?

ARSI ensures regulatory compliance in method development by adhering to guidelines set by the International Council for Harmonisation (ICH), the United States Pharmacopeia (USP), and other relevant regulatory bodies. Our methods are developed and validated to meet the stringent requirements of regulatory agencies worldwide.

Can ARSI develop stability-indicating methods?

Yes, ARSI specializes in developing stability-indicating methods. These methods are designed to detect and quantify degradation products and impurities under various stress conditions, ensuring the stability and shelf-life of drug products. Our stability-indicating methods are crucial for regulatory submissions and quality assurance.

What are the key benefits of choosing ARSI for method development?

Choosing ARSI for method development offers several key benefits: access to experienced scientists, advanced analytical technologies, customized solutions, comprehensive validation, regulatory compliance, and a client-focused approach. ARSI is dedicated to delivering high-quality, reliable, and timely analytical services.

Discuss your drug discovery & development needs, get a custom quote today!