The end of 2022 brought another regulatory deadline – Kuwait announced mandatory serialization until 2024. Market overview Kuwait's Pharmaceuticals market is in the growing stage thanks to the government`s healthcare initiatives. Due to large investments through public-private partnerships for the development of the healthcare sector, the pharma...
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Discover the pharmaceutical compliance requirements for Kazakhstan and the critical essentials regarding Track & Trace in the region. Download the whitepaper now by filling in the fields below: [contact-form-7 id="12909" title="Contact form - Whitepaper Kazakhstan Regulation"]...
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Discover the pharmaceutical compliance requirements for Kyrgyzstan and the key essentials regarding Track & Trace in the region. Download the whitepaper now by filling the fields below: [contact-form-7 id="12904" title="Contact form - Whitepaper Kyrgyzstan Regulation"]...
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This year pharma industry will face new regulatory requirements for Kyrgyzstan, Kazakhstan, Saudi Arabia, UAE, USA and Australia. Regulatory Compliance is a permanent hot topic for all supply chain participants.2023 is bringing new challenges regarding the track and trace requirements. Here are the essentials of the...
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Discover the SFDA requirements and Track & Trace specification for Saudi Arabia Saudi Arabia is one of the most dynamically developing Pharma markets in the MENA region. The market is estimated to reach USD 11 billion in 2026, almost as big as Egypt and the UAE...
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The government of Kyrgyz Republic has taken measures against drug counterfeiting, including the medicines in the binding product list for labelling. As early as 2019, the Kyrgyz Republic Government issued Decree No. 470/12.09.2019 for the “Product Marking identification in the Kyrgyz Republic” and Decree No. 554/17.10.2019...
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Discover the pharmaceutical compliance requirements for UAE and the key essentials regarding Track & Trace in the region. Download the whitepaper now by filling the fields below: [contact-form-7 id="12797" title="Contact form - Whitepaper UAE Regulation"]...
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More than a year after MDR went live, supply chain participants already discovered the benefits together with the challenges Medical Devices Regulation (MDR) was one of the key moments in 2021 to establish traceability enhancement from Manufacturers to Patients. And one year later, the interest remains...
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Discover Track & Trace Requirements for Australia Till January 2023, the serialization and use of data matrix are optional for manufacturers and sponsors supplying medicines in Australia. The Therapeutic Goods Order - Standard for labels of prescription and related medicines (TGO) No.91 and TGO No.92 documented...
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Tatmeen, UAE`s Traceability system, is in the final stretch of officially going into force From 13th December 2022, all participants involved in manufacturing, distributing and dispensing pharmaceutical products must be ready with the Serialization and Track and Trace (T&T) requirements. The legislation was published by UAE`s...
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