Stability Study of Pharmaceuticals Product
A stability study is one of the quality parameters and is carried out to determine the ability of a product to resist within its defined specifications throughout the period of storage and use.
Generally, the stability test involves various treatments, such as temperature, relative humidity, and exposure to light. This study is conducted by placing the product in a chamber that is controlled in temperature, humidity, and light intensity.
How SIG can help
SIG laboratory provides stability testing services for pharmaceutical products. This testing service helps to determine the product quality in a certain treatment.
Method of Analysis
Stability studies need to be supported by well-controlled product storage conditions. Generally, this is conducted using a climatic chamber. The use of a climatic chamber with appropriate performance will assist you in interpreting the shelf-life of your product.
Library of Knowledge
SIG Supports the 2025 ASPAKI National Meeting for the Advancement of Indonesia’s Medical Device Industry
Jakarta, January 15, 2025 – SIG has once again demonstrated its commitment to supporting the growth of Indonesia's medical device industry by participating as a sponsor in the National Conference (Munas) of the Indonesian Medical Device Manufacturers Association...
Understanding the New BPOM Regulation on Contaminant Limits in Cosmetics: What Do We Need to Know?
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SIG once again demonstrated its active involvement in international forums by attending the Waters ASEAN Food Summit 2024, a global platform uniting governments, industries, and academia to foster strategic partnerships aimed at enhancing food quality and safety...
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