Quality Control & Quality Assurance

The system of QA/QC at ASPO Pharmaceuticals LLP ensures that:

1. Pharmaceutical products are designed and developed in a way that takes account of the requirements of WHO- GMP and other associated codes such as good laboratory practice (GLP) and good clinical practice (GCP).

2. Production and control operations are clearly specified in a written form and WHO-GMP standards are ensured.

3. Managerial responsibilities are clearly specified in job descriptions.

4. The finished product is correctly processed and checked according to the defined procedures.

5. Pharmaceutical products are not sold or supplied, before the authorized person have certified that, each production batch has been produced and controlled, in accordance with the marketing requirements and any other regulations, that are  relevant to the production control and release of pharmaceutical products.