We've curated a range of generic medicines that not only promise quality but also offer you the advantage of affordable pricing. Each generic is manufactured at a WHO GMP-approved and certified plant, meticulously tested, stored and transported to ensure that you get the best quality product along with the generic price advantage.
We invite you to verify the quality of our medicines by entering the details of your medicine below and instantly accessing the Certificate of Analysis (CoA), which is a testament to our commitment to your health and well-being and the rigorous testing and standards adhered to in the creation of generic.
Welcome to Aus Pharma
What is the Certificate of Analysis (CoA)?
A Certificate of Analysis (CoA) is an assurance given to the customers, manufacturers, and suppliers that the product they are dealing with meets their agreed-upon standards. The COA is provided by the manufacturer and certifies that the medicine has been tested against the quality parameters. As part of this, each product is tested for multiple parameters against a standard (reference) defined by the Indian or International pharmacopoeia.
What are the testing parameters in a Certificate of Analysis?
Description
Describes the product, shape colour, type of coating, scored or unscored tablet.
Identification
The product is tested to match the retention time against the standard (reference defined by the regulatory authority). If the retention time matches, it means that the product is in compliance with standard product.
Average Weight
The Average weight required for the product to meet the standards.
Uniformity Of Weight
Test of uniformity of weight (mass) is carried out for tablets and capsules to ensure that the accurate and consistent dosage form is administered to patients
Hardness
This test determines the breaking point or the force required to break a tablet. This measurement is essential to assess the tablet's resistance to stress and to ensure consistent quali- ty and performance. Softer tablets
Thickness
The thickness is tested to ensure therapeutic efficacy since it impacts the disintegration and dissolution be- haviour. In addition, thickness can be a useful indicator of the consistency, which ensures the dose uniformity.
Length
Tests if the product is within the length range defined under the standard specifications.
Width
Tests if the product is within the width range defined under the standard specifications.
Friability
This test determines the stress-with- standing capability of the product and is an important criterion to ensure that the product reaches the consumers in intact condition.
Disintegration
This test measures how quickly the tablet breaks down into smaller particles, allowing for a greater sur- face area & availability of the drug when taken by a patient. This test is of critical importance to achieve a
Dissolution
Dissolution testing measures the extent & rate of solution formation from a dosage form, such as tablet, capsule, ointment, etc. The dissolu- tion of a drug is important for its bio- availability & therapeutic effective-
Uniformity Of Content
This test verifies the limit on the product variance within each tablet or capsule. The intention is to make sure that products do not have an abnor- mally low or high amount of the active ingredient. It helps to ensure that the
So what does it mean for you?
A product that complies with the specifications of the standard product (reference) in the Certificate of Analysis testing indicates that the product is at par with the standard product.
Your health is our priority, and with our generics, you can trust that we're committed to delivering the best quality products.