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 |
Services
Raw Materials
Packaging Materials
In-Process Materials
Finished Products
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.
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.