Pharmaceutical professionals have extensive knowledge to analyze the raw materials, processes, and finished products to determine the safety and efficacy of a new drug. Pharmaceutical quality assurance is a crucial practice in the manufacturing practice. This is where pharmacopeias come into play.
Pharmacopeias are documents designed to provide public standards relating to the quality, safety, and efficacy of a drug. Today, pharmacopeias play a major role in the regulatory process and control of pharmaceutical ingredients. Analysts for pharmaceutical quality assurance will draw upon these standards in their methods of quality control. With the global expansion of drug manufacturing and standards, professionals in the quality field are in demand across Canada and the world. Let’s take a closer look at the role of pharmacopeias for those interested in the evolving industry.
The Globalization of Pharmaceutical Quality Assurance
A globalized pharmaceutical industry requires globally harmonized pharmacopeias. To enable free movement and trade of drugs across different countries, the pharmaceutical industry needs to develop global quality standards of medicine.
Pharmacopeias aim to define product quality and improve the application of these standards by pharmaceutical companies worldwide. Pharmacopeias encourage:
- A globally established reputation and policies
- A high degree of visibility
- Open communication with stakeholders and partners
In the context of a globalized pharmaceutical industry, pharmacopeias offer quality and safety standards to protect public health and facilitate the expansion of international trade. As a global regulatory system, they have the power to provide mutual recognition when it comes to assessments by licensing authorities. Students in pharmaceutical courses in Toronto will study global regulatory strategies to understand the global requirements as well as the impact of regulatory changes that affect the pharmaceutical industry.
Ensuring Health and Safety
Pharmacopeias also play an important role in the move against falsified medicines. Pharmacopoeia commissions are responsible for protecting public health against error or fraud in the field of medicine. They work by defining the standards with which a new drug must comply when proposed for medicinal use and laying out the methods by which compliance can be judged.
With the globalization of pharmaceuticals, the counterfeit of medicines has become a growing threat to public safety. Pharmacopeias can reduce the occurrence of this by:
- Identifying potential adulterations or impurities
- Adjusting its standards to meet market developments
- Revising monographs quickly
It’s important to note, however, that the prevention of drug counterfeiting for pharmaceutical quality assurance can not be achieved solely by pharmacopeias. Rather pharmacopeias are one tool among many that can help the overall success of international cooperation in ensuring the safety of medicinal products.
Encouraging Pharmaceutical Innovation
While pharmacopeias must define strict quality standards, they must also allow for sufficient flexibility to pave the way for pharmaceutical innovations. For example, pharmacopeias should allow for the implementation of analytical technology in the production and control stages of new drugs. Regulations must consider the various needs of the global pharmaceutical industry as well as different enterprises, all while bearing in mind public safety concerns.
Pharmacopeias should work to develop a drug that can meet the various requirements of the market. When applied effectively, pharmacopeias can:
- Reduce the time needed for innovative medicines to become available to the public
- Maintain global quality standards
- Facilitate the geographical expansion of medicinal products
With knowledge of how pharmacopeias can impact an evolving industry, pharmaceutical students can open their path to a global career.
Are you looking to earn your pharmaceutical quality assurance diploma?
Contact AAPS today!