Harmonizing Global Efforts Against Counterfeits - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Harmonizing Global Efforts Against Counterfeits


Pharmaceutical Technology
Volume 36, Issue 12

In addition to globalisation, high financial rewards and low penalties for counterfeiters are contributing to the rise in fake medicines. Although some progress has been made in several countries to address drug counterfeiting, success is variable and, despite seeing a reduction in counterfeiting for (e.g., Pfizer’s success in reducing Viagra counterfeits), the problem has not been eradicated.

Tighter regulations have helped improve the detection of counterfeit products at various stages of the supply chain and prosecutions appear to be increasing. Pharmaceutical manufacturers, while working to comply with the numerous and varied regulations to prevent counterfeiting, have also undertaken their own initiatives to protect their brands. For example, companies are applying radio-frequency identification (RFID) tags to individual packages and using covert (e.g., tagents, holograms, colour shifting inks) and overt (e.g., tamper-evident seals, barcodes) methods.

However, one method alone is usually not sufficient to prevent counterfeiting, says Janice Kite, traceability director of GS1 Healthcare.

PharmTech spoke to Kite about global collaboration to address these challenges. GS1 is an international not-for-profit association with member organisations in more than 100 countries. The association is dedicated to the design and implementation of global standards and solutions to improve the efficiency and visibility of supply and demand chains globally and across sectors. Part of the association involves GS1 Healthcare, which is a voluntary global healthcare user group that brings together stakeholders from pharmaceutical and medical-device companies; wholesalers, purchasers, and distributors; hospitals and pharmacies; logistics providers; and governmental and regulatory bodies. The mission of GS1 Healthcare is to lead the healthcare sector to the successful development and implementation of global standards that enhance patient safety and supply-chain efficiencies.

GS1 has developed a system of standards (available at http://www.gs1.org/docs/GS1_System_of_Standards.pdf) that is meant to be used by stakeholders as a best practice for increasing supply-chain security and improving patient safety. According to Kite, regulators in Turkey, Argentina, and Australia are currently following the GS1 system of standards, and many pharmaceutical companies are already using the GS1 standards for the identification of their products.


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

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

Survey
How does your company apply quality-by-design (QbD) principles to manufacturing processes?
To all processes for both new and legacy products
To all process for new products only
To select process for new products only
To select processes for both new and legacy products
Do not use QbD
To all processes for both new and legacy products
18%
To all process for new products only
13%
To select process for new products only
22%
To select processes for both new and legacy products
22%
Do not use QbD
24%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Inadequate Access to Medicines Puts EU at Risk
FDA Offers Insight on QbD for Modified-Release Products
Global Biosimilars Market to Reach $2.445 Billion in 2013
Adapting to Change
AstraZeneca and Exco InTouch Collaborate to Augment Current COPD Pathways
FindPharma Custom Search
Source: Pharmaceutical Technology,
Click here