Extraordinary commitments by the pharmaceutical industry and the US Food and Drug Administration aim to ensure that prescription
drugs sold in the US and throughout the supply chain are completely safe. Both FDA and industry continuously pursue every
means available to help guarantee that the medicines patients and practitioners receive are of the highest quality.
As FDA Commissioner Margaret Hamburg noted in February 2010 at the Center for Strategic and International Studies, all people
of the world deserve access to safe food and quality medical care. She also noted that FDA is a critical player, domestically
and internationally in promoting and protecting the health of the public.
With the contaminated heparin incident in 2008, it became apparent that those individuals intent on deliberately adulterating
drug products were finding sophisticated means of operating. And while such incidents are rare, the realities of a globalized
pharmaceutical marketplace have resulted in challenges and opportunities for industry and FDA to develop systems to protect
the quality of the materials used in drug manufacturing and the security of products as they move from the original source
to the end user. Approximately 4 billion prescriptions were dispensed in the US in 2009, according to IMS Health. That number
equates to several billions of tablets, capsules, liquids, injectables, inhalation units, and other dosage forms, and the
active ingredients used in making them, moving through the supply chain. However, the Generic Pharmaceutical Association (GPhA)
believes that careful vigilance by FDA, manufacturers, and supply-chain stakeholders can keep the prevalence of drug contamination
and intentional adulteration low.
Proactive efforts to protect consumers from counterfeit drugs also must be a priority. Although most drugs, including the
generic drugs that account for 75% of all prescriptions dispensed in the US, are seldom targeted by counterfeiters, counterfeit
versions of some of the most expensive prescription medicines continue to appear in the marketplace. Many of these counterfeit
versions are sold over the Internet with little or no regulatory control. Counterfeit drugs present a significant risk to
public health, not only because they are unapproved, but also because they fail to deliver the needed therapeutic effect to
Keeping counterfeit and contaminated drugs out of the US supply requires a dual effort spearheaded by FDA and industry. Only
through corporative and coordinated action can the necessary oversight and controls be capable of maintaining drug security.
For instance, the new border-control initiative developed by FDA is an excellent endeavor to curtail the incidence of poor
standard medicines entering the US from other countries. This program, Predictive Risk-based Evaluation for Dynamic Import
Compliance Targeting (PREDICT), encompasses a border-based method that assesses drugs at the point of import. Barcodes on
cases of medicines will be scanned at US points of entry and linked to a central database.
As a result, FDA border agents will know immediately whether the producer has a license to ship and sell drugs into the US.
If the products do not meet FDA compliance, they will not be allowed passed the borders. For its part, the pharmaceutical
industry uses multiple strategies to prevent counterfeit drugs from entering the US supply chain, including comprehensive
vender audits, robust controls of the supply chain, monitoring and control of qualified shipping channels to name a few.
Supply-chain and testing controls
Regarding the supply and distribution, manufacturers must continue their robust testing and supplier oversight to ensure that
quality is built into the process. Innovator-drug firms operate in a highly regulated environment, and rightly so. Makers
of finished dosage forms methodically and meticulously evaluate the plants, manufacturing practices, and quality control capabilities
of their suppliers' inactive and active ingredients suppliers.
These company-led assessments provide the foundation for drug-product quality by ensuring that prudent and deliberate steps
are taken to eliminate potential contamination or adulteration in distribution channels. Moreover, manufacturers test incoming
raw materials for quality, purity, and potency in accordance with FDA-approved analytical methods. The test methods in place
are designed to ensure that all active ingredients and other raw materials meet their predetermined quality attributes. Finished-dosage
manufacturers also perform sophisticated testing during the manufacturing process that helps to verify that prescription medicines
delivered to consumers and patients meet all standards for quality, purity, and potency.