Skip to main content Skip to search Skip to main navigation

Swissmedic: Data on imports of illegal medicinal products via the internet

On 4 March 2021, Swissmedic announced the numbers on medicinal products illegally imported into Switzerland. In 2020, 6733 illegal imports were recorded. Compared to the previous year, the number has decreased only slightly.  Among the countries of origin, Singapore has replaced India, which has long been in the lead. It was followed by Western European countries such as the UK and Germany in particular.

Singapore is increasingly being used as a hub by suppliers of illegal medicinal products.

Which falsified medicinal products represent the majority?

Erectile stimulants continue to top the list, followed by other prescriptive medicinal products as well as sleeping pills and tranquilizers such as Xanax and Valium.

Swissmedic also warns against supposedly herbal products that, however, contain undeclared chemical active ingredients. They are advertised, especially in social media, as "herbal" and "natural" products for potency enhancement or for weight loss. Delivery often comes without a patient information leaflet or cardboard packaging.

A suspicion of an illegal drug should be reported to Swissmedic via the Medicrime contact form.

Successes in the fight against falsified medicinal products

In October 2020, German customs and the Bavarian Cybercrime Central Office succeeded in smashing a global network of illegally operating dealers in the "Hydra" investigation complex. Two people were arrested in the process. The international investigation lasted almost two years. The falsified preparations were assembled in a warehouse in Singapore, shipped by mail and sent by air freight.


Sources:

Swissmedic: Illegal imports of medicinal products in 2020: medicines from the internet are still in demand

Attorney General's Office Bamberg: Zoll und ZCB zerschlagen im Ermittlungskomplex „Hydra“ weltweites Netzwerk von Händlern illegaler und nicht zugelassener Arzneimittel – Zwei Haftbefehle vollstreckt (in German)

Meet the GMP Compliance Adviser

The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business. 

The demo access is non-binding and ends automatically.

Test it now for free

You may also be interested in the following articles:

EMA: Revision of Annex 6 - Manufacture of Medicinal Gases

EMA: Revision of Annex 6 - Manufacture of Medicinal Gases

EMA and PIC/S have published a concept paper announcing a targeted revision of Annex 6 Manufacture of Medicinal Gases of the EU GMP Guide. The last update dates from 2010. The revision aims to reflect current manufacturing practice, technological progress and lessons learned from the COVID-19 pandemic.

Read more
EMA: Concept Paper on the Revision of Annex 15

EMA: Concept Paper on the Revision of Annex 15

EMA and PIC/S have published a concept paper outlining a targeted revision of Annex 15 (Qualification and Validation).

Read more
What do Typical Manufacturing Processes for Sterile Products look like?

What do Typical Manufacturing Processes for Sterile Products look like?

Here's the answer:
Read more
Human Resource Management as a Key to Success

Human Resource Management as a Key to Success

The pharmaceutical industry in Germany and other countries, too, faces considerable challenges in the area of human resource management. These problems have far-reaching implications for the competitiveness and innovative power of the industry.

Read more
EMA: Reflection Paper on the Qualification of Non-Mutagenic Impurities (NMIs)

EMA: Reflection Paper on the Qualification of Non-Mutagenic Impurities (NMIs)

The EMA has published a new reflection paper outlining its current thinking on the qualification of non-mutagenic impurities (NMIs). The paper addresses recommended approaches for evaluating the safety of new or increased impurity levels, particularly when such impurities exceed the ICH Q3A/Q3B qualification thresholds and are identified after completion of non-clinical toxicology studies.

Read more
EMA: Discussions on the Revised ERA Guideline

EMA: Discussions on the Revised ERA Guideline

During the second industry stakeholder webinar on the revised guideline on environmental risk assessment (ERA) for medicinal products for human use, the European Medicines Agency (EMA) addressed key implementation challenges observed during the first year of application.
Read more
Previous
Next