We provide a full range of services for GMP Quality Control Testing and Release/Reject programs for Raw Materials, Packaging Materials, In-Process Materials and Finished Products.

For brands, Quality Control Testing is the pivotal activity that can delay the next step in a production cycle. For example, the qualification of a raw material may impede compounding operations, or the verification of label claim may delay product shipments.

You can take comfort in knowing that our quality programs adhere to and surpass all Canadian government quality control testing standards and protocols meet consumer safety requirements.

Quality Control Program

  • Verification of individual ingredients or final product standards
  • TO verify consistent levels of active ingredients in your product
  • Meet compliance with Health Canada, GMP and industry standards
  • Confirm marketing claims at product release

Products Tested

  • Raw Materials
  • Packaging Materials
  • In-Process Materials
  • Finished Products

Release/Reject Program

At the heart of quality control testing and all Good Manufacturing Practices (GMP) is the Release/Reject program. This program requires the generation, review and acceptance of analytical data in many cases to release products from a Quarantine Status to a Released Goods Status for sale.

Quality Control Testing Services

Raw Material (RM) Testing and Identification Active Pharmaceutical Ingredients (API’s) Pharmaceutical Intermediates
Excipients Trace Contamination Identification Stability
Method Transfer, Validation & Development Drug Stability Testing for Liquid and Injectables Organic Volatile Impurities
Assay (HPLC, GC, UV-Vis), AA TLC/HPLTC Disintegration
FTIR Dissolution Studies Cleaning Validations
Content Uniformity Metal Analysis/Heavy Metals Melting Point
Viscosity Compendial Tests Solubility
pH and Titrations Water Testing Conductivity
Karl Fischer/LOD Moisture Analysis Residual Solvents
Optical Rotation Food Allergens Dissolution Enzymes Assay
Pesticides Phobiotics Assay In-Process Testing Finished Product Release
Raw Material (RM) Testing and Identification
Active Pharmaceutical Ingredients (API’s)
Pharmaceutical Intermediates
Excipients
Trace Contamination Identification
Stability
Method Transfer, Validation & Development
Drug Stability Testing for Liquid and Injectables
Organic Volatile Impurities
Assay (HPLC, GC, UV-Vis), AA
TLC/HPLTC
Disintegration
FTIR
Dissolution Studies
Cleaning Validations
Content Uniformity
Metal Analysis/Heavy Metals
Melting Point
Viscosity
Compendial Tests
Solubility
pH and Titrations
Water Testing
Conductivity
Karl Fischer/LOD
Moisture Analysis
Residual Solvents
Optical Rotation
Food Allergens
Dissolution Enzymes Assay
Pesticides Phobiotics Assay
In-Process Testing
Finished Product Release
Request Services

Regular Service for routine sample turnaround time is 7- 10 business days.
Rush Service available for 5 day and 2 day turnaround at additional rates.

Request Services

Regular Service for routine sample turnaround time is 7- 10 business days. Rush Service available for 5 day and 2 day turnaround at additional rates.