AALL
SERVICES
Test Method Development.
We have extensive experience in developing analytical test methods for various applications and across a variety of product types in compliance with international regulations. We can assist throughout the entire method development activity to meet your requirements. This includes project planning, protocol writing, execution, and final development reports to satisfy your regulatory needs.
Test Method Validation.
We have extensive experience in validating analytical test methods for various applications and across a variety of product types in compliance with international regulations. We can assist throughout the entire method validation activity to meet your requirements. This includes project planning, protocol writing, execution, statistical evaluation and final validation report writing to satisfy your regulatory needs.
Finished Product Testing
We specialize in offering GMP compliant pharmaceutical testing services. We have the ability to perform a vast array of analysis on pharmaceutical finished products, raw materials, and other ingredients, from a variety of compendiums.
These include:
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The European Pharmacopoeia (EP)
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The British Pharmacopoeia (BP)
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The United States Pharmacopoeia (USP)
Dissolution Profiling.
Dissolution is a critical parameter of pharmaceutical dosage forms. It is well recognized that in-vitro dissolution testing is relied upon to screen formulations during development and to ensure batch-to-batch quality control during routine release testing. Dissolution is the process by which a solid solute enters into solution in the presence of the solvent. Dissolution rate may be defined as the amount of active ingredient in a solid dosage form dissolved in unit time under standardized conditions of liquid/solid interface, temperature and media composition.
Technical Projects.
AALL has extensive analytical testing and technical support services to assist pharmaceutical and healthcare clients achieve their regulatory registration goals and technical troubleshooting. We always solve problems quickly and accurately, backed up by clear communication with clients.
cGMP Laboratory Facilities.
We have an advanced range of equipment for analytical and physical chemistry analysis to support both technical projects and routine GMP compliant QC testing. We recognize that the quality and capability of our laboratory facilities are of great importance. This is why we put continuous investment into our world-class facilities to ensure we deliver exceptional value to all our clients.