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CGMP / WHO GMP Certifications
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A basic principle of Current Good Manufacturing Practices (cGMP) is that quality cannot be tested into a batch of product but must be built into each batch of product during all stages of the manufacturing process. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
- Unexpected contamination of products, causing damage to health or even death.
- Incorrect labels on containers, which could mean that patients receive the wrong medicine.
- Insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects.
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