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Stability testing

Activ Pharmaceuticals has the expertise and the necessary environmental facilities to undertake accelerated and full time stability studies for their clients. All new products are subjected to preliminary, accelerated stability testing as well as preservative efficacy where appropriate. Full time stability testing is conducted by individual arrangement.

Under the current GMP guidelines, therapeutic products must be placed on a program of on-going, follow up stability studies. Activ Pharmaceuticals can assist its clients to meet this regulatory obligation by undertaking such testing in-house at very favourable commercial rates.

Activ Pharmaceuticals may also conduct a stability program for the client for the purpose of Listing or Registering a new therapeutic product. In such cases, we will generate the data and compile the finished report to the nominated regulatory affairs body for submission.