Daphne Allen

January 13, 2017

2 Min Read
Pharma firms 'on the hook' with Brazil's new law on serialization, says Pharmapack speaker
Image source: Shutterstock; Copyright: Harvepino

Late 2016 was a busy season for Brazil, as the end of the year saw several developments in Brazil’s serialization program for medicines, Peter Schmitt, Managing Director & Co-Founder of Montesino Associates, tells PMP News.

Schmitt will be sharing the latest news in “Regulatory Serialization Guidelines and Implications in Brazil” at the upcoming February 1 “Serialisation, Track & Trace Symposium” at Pharmapack Europe.

For instance, the laws in Brazil have changed. “As a result of a lawsuit filed by Abrafarma on Tuesday, September 29, 2016, Anvisa’s Board of Directors suspended Article 23 of RDC 54/2013. This article had required the serialization of all drugs sold in Brazil by December 10, 2016,” says Schmitt. “Law 13.410/2016 (PL 4069/2015) was approved by the Brazilian legislature in October and signed into law on December 28, 2016. The law amends Law 11.903/2009, which established the SNCM (National Drug Control System).”

Schmitt explains that the new law extends the timeline for implementation of the regulation and implements a centralized database administered by Anvisa to manage serialization data.

Consequently, Anvisa now has “a fixed amount of time to published detailed instructions, starting with a Public Hearing,” Schmitt says. “Once those regulations are published, the new law provides fixed amounts of time for pilot testing, serialization, and full traceability of medicines sold in Brazil.”

Schmitt will explore these changes along with the history of Brazil’s serialization regulations. He will provide:

• Review of prior serialization regulations

• Analysis of new regulations

• The timeline for implementation

• Comparison with United States and Europe

“The Pharmapack talk will analyze the new law and the new timeline, highlighting what has changed, what remains the same, and what is still to be determined,” Schmitt says. “The law specifies milestones in the process and requires Anvisa to finalize technical regulations at the beginning of the process. The talk will explore those details that are already finalized and review questions awaiting the final regulations from Anvisa.”

To pharmaceutical companies, Schmitt says, “You are on the hook!

“Given the complexity of the issues surrounding serialization and traceability, it is not surprising that Brazilian lawmakers and regulators found it necessary to modify the initial program," he continues. "Similarly, now is the time for pharmaceutical manufacturers who sell medicines in Brazil to implement serialization programs. The talk will briefly highlight guidelines for effective program implementation and potential benefits for pharmaceutical manufacturers once serialization begins.”

Please visit www.pharmapackeurope.com to register for the event.

About the Author(s)

Daphne Allen

Daphne Allen is editor-in-chief of Design News. She previously served as editor-in-chief of MD+DI and of Pharmaceutical & Medical Packaging News and also served as an editor for Packaging Digest. Daphne has covered design, manufacturing, materials, packaging, labeling, and regulatory issues for more than 20 years. She has also presented on these topics in several webinars and conferences, most recently discussing design and engineering trends at IME West 2024 and leading an Industry ShopTalk discussion during the show on artificial intelligence.

Follow Daphne on X at @daphneallen and reach her at [email protected].

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