Reliable Analytical Testing to Support Pharmaceutical Product Quality

Medicap Laboratories provides pharmaceutical analytical testing services supporting product development, manufacturing, quality control, and regulatory requirements.

Our analytical laboratory is equipped with a range of analytical instrumentation and supported by experienced technical personnel and quality systems.

Discuss Your Testing Requirements

Analytical Testing Capabilities

Our laboratory capabilities support pharmaceutical products throughout their development and manufacturing lifecycle.

  • Raw Material Testing

  • In-process testing

  • Finished product testing

  • Assay testing

  • Dissolution testing

  • Identification testing

  • Impurity testing

  • Stability testing

  • Method development

  • Method validation

  • Cleaning verification and validation support

Analytical Instrumentation

Our laboratory capabilities include instrumentation such as:

HPLC
High-performance liquid chromatography for assay, impurities, and related analytical testing.
GC
Gas chromatography capabilities supporting applicable pharmaceutical testing requirements.
FTIR
Fourier-transform infrared spectroscopy for identification and characterization.
UV/VIS
UV/Visible spectrophotometry for applicable quantitative and qualitative testing.

Analytical Support Throughout the Product Lifecycle

Our analytical team can support customers at multiple stages:

  1. 01

    Product Development

    Analytical testing during formulation and process development.

  2. 02

    Manufacturing

    Testing and in-process monitoring supporting manufacturing operations.

  3. 03

    Quality Control

    Testing of raw materials, intermediates, and finished products.

  4. 04

    Stability

    Analytical support for stability programs and product shelf-life evaluation.

  5. 05

    Regulatory

    Analytical data and documentation supporting pharmaceutical regulatory activities.

Method Development & Validation

Analytical methods are an important component of pharmaceutical development and quality control.

Our team can support method development and validation activities based on product requirements and applicable regulatory expectations.

Stability Testing

Stability testing provides critical information about how pharmaceutical products perform over time under defined storage conditions.

Our analytical capabilities can support stability programs for pharmaceutical products and generate data required for product development and regulatory activities.

Why Choose Medicap Analytical Services?

  • Integrated with pharmaceutical manufacturing

  • Experienced technical team

  • Multiple analytical platforms

  • Support from development through commercial production

  • Quality-focused processes

  • Canadian pharmaceutical facility

FAQ

  • What analytical instruments does Medicap have?

    Our laboratory includes HPLC, GC, FTIR, and UV/VIS instrumentation, among other analytical capabilities.

  • Do you provide dissolution testing?

    Yes. Dissolution testing can be performed as part of applicable pharmaceutical analytical programs.

  • Does Medicap perform stability testing?

    Yes. We provide analytical support for pharmaceutical stability programs.

  • Can you test products manufactured elsewhere?

    Analytical testing projects can be evaluated based on the product, specification, method, sample requirements, and applicable quality considerations.

  • Do you provide analytical method development?

    Yes. Analytical method development and validation support can be provided based on project requirements.

Contact Us

Looking for a Pharmaceutical Analytical Testing Partner ?

Share your product, testing requirements, specifications and timeline with our team.

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