Can Pharma Keep Pace With The Counterfeiters? - Pharmaceutical Technology

Latest Issue

Latest Issue
PharmTech Europe

Can Pharma Keep Pace With The Counterfeiters?

Pharmaceutical Technology Europe
Volume 22, Issue 7

The full version of this counterfeiting feature can be read in the July issue of our digital magazine:

The problem of counterfeit medicines was first addressed at an international level in 1985, when a conference of experts recommended that the World Health Organization (WHO), together with other international and non-governmental organisations, should study the feasibility of setting up a clearing house to collect data and to inform governments about the nature and extent of counterfeiting. Since then, however, the problem has only escalated. According to the WHO, the magnitude of the issue is difficult to assess because of the variety of information sources available.1 Additionally, the WHO stresses that counterfeiters are extremely flexible and can change their methods from day to day, so the results of a study may already be out of date the day they are released.

Jason Hosking/Getty Images
However, the statistics that are available show unsettling results. For example, compared with 2005, seizures of counterfeit medicines at the EU border increased by 380% in 2007.2 Meanwhile, research commissioned by Aegate revealed that 5% of consumers across five European countries suspect they may have received a counterfeit prescription drug.3 The research adds that the majority of consumers believe that the trade in counterfeit medicines is largely the responsibility of the manufacturer.

Fortunately, the threat of counterfeits has prompted the development of a number of anti-counterfeiting solutions, from simple holograms and watermarks, to sophisticated barcodes that enable track and trace, tagged packages, and even technologies that can be applied directly to individual tablets. But which solution is most widely used by the pharma industry?

Figure 1
To get a better idea, PTE conducted a survey4 of industry executives and found that, although barcoding and tamper-evident packaging was the most popular solution in use amongst those surveyed, astonishingly, the majority of respondents (27%) admitted that their company had yet to instate an anti-counterfeiting solution (Figure 1).

Products can never be made completely secure against counterfeiting; however, counterfeiters will always target medicines that are easiest to copy. In the EU, companies that have yet to implement a solution are going to have to move quickly in light of the significant threat that counterfeiting presents as well as amendments that are being made to the current EU anti-counterfeiting directive; one of which mandates safety features, such as seals or serial numbers, for certain medicines.5

Speaking to a variety of industry leaders, PTE examines some of the trends in anti-counterfeiting technologies, as well as the innovative solutions being used by the industry.


1. WHO, Medicines: counterfeit medicines, Fact sheet N275 (2010).

2. European Commission, Counterfeit Medicines (2010).

3. Aegate, Medicines top counterfeit concern list in Europe — consumers call for tougher safety measures (2009).


5. European Parliament, Fake medicines: MEPs want to target online sales (2010).


blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
| Weekly

FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
Ebola Outbreak Raises Ethical Issues
Better Comms Means a Fitter Future for Pharma, Part 2: Realizing the Benefits of Unified Communications
Better Comms Means a Fitter Future for Pharma, Part 1: Challenges and Changes
Source: Pharmaceutical Technology Europe,
Click here