Tag: Quality control

The global dietary supplement market is projected to reach over $300 billion in the coming years, with many consumers asking, "Are Swanson vitamins made in China?". The answer is more complex than a simple yes or no, involving a global network of sourcing partners and a multi-layered approach to manufacturing and quality control.

According to the company, most Nature Made products are manufactured in the United States at their own facilities in Southern California and Alabama. While the finished products are primarily made domestically, this does not answer the question of where the raw ingredients are sourced, which is a common concern when asking, "Are Nature Made supplements made in China?".

With high rates of drug candidate attrition in clinical development, a thorough understanding of **what is characterization of a drug?** is paramount for ensuring a successful and safe final product. This comprehensive analysis of a drug's properties is a cornerstone of pharmaceutical science, underpinning the entire lifecycle of a medication from discovery to market.

According to the National Institutes of Health, eye drops represent up to 90% of all commercially available ophthalmic drug products, making the methods of preparation of eye drops critically important for patient safety and efficacy. These preparations are complex, sterile formulations designed to deliver medication directly to the surface of the eye while minimizing contamination risks and ensuring patient comfort.

Developed over 140 years ago by Danish chemist Johan Kjeldahl, the Kjeldahl method remains a globally recognized analytical technique for determining nitrogen content in various materials, including pharmaceutical products. In pharmacy, **what is Kjeldahl method in pharmacy?** is a key question that relates to quantifying nitrogen, which serves as a proxy for protein content or is a component of active pharmaceutical ingredients (APIs) and excipients. This comprehensive guide explores the principle, procedure, and specific applications of this robust analytical process within the pharmaceutical industry.

In the highly regulated pharmaceutical industry, every batch of medication or raw material must be tested rigorously for quality and purity. A Certificate of Analysis, or COA, is a document that encapsulates the results of this crucial testing, serving as a pillar of patient safety and regulatory compliance.

According to Good Manufacturing Practices (GMP), every batch of a drug product must have a comprehensive record. This critical document, known as the **Batch Production and Control Record (BPCR)**, ensures product quality, safety, and regulatory compliance throughout the manufacturing process.

Regulatory bodies like the FDA consistently cite inadequate Corrective and Preventive Action (CAPA) processes as a leading cause of enforcement actions. So, **what is capa in pharma**? It is the bedrock of quality management, a structured, systematic process for investigating and resolving quality issues while preventing their recurrence.

While the term GPT is now widely associated with artificial intelligence (AI), in the context of pharmacy, it has at least three distinct meanings spanning clinical diagnostics, quality control, and cutting-edge technology. Understanding **what does GPT stand for in pharmacy** requires differentiating between these contexts to avoid confusion and properly apply the term.

Headquartered in Palm Beach Gardens, Florida, Garden of Life utilizes a network of third-party certified facilities within the United States for the manufacturing of its products, while sourcing ingredients globally. The company places a strong emphasis on traceability and extensive third-party testing to ensure quality control, transparency, and product purity.