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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Cloud solutions build a scalable IT environment for Pharmaceuticals, transforming and benefiting the whole business processes. Overview During the last few years, the pharma industry has had to rethink the approaches and working models commonly used. Digital transformation is still a hot topic in the supply chain....
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The invention of barcodes changed the Pharma industry and made traceability achievable. In your everyday life, you usually don’t notice that barcodes are everywhere – on your food, medicines, water, etc. There is a reason why they are there. Barcodes have a significant role in the...
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Almost 1 year after Uzbekistan`s Decree 737 for the establishment of obligatory digital labeling, pharma supply chain participants meet the first deadline for mandatory serialization. On the first day of September, also came the first deadline for the serialization of medicines in Uzbekistan. Earlier in April,...
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An innovative technology solution could help reduce environmental impact while serving your business processes It is easy to say “we go green”, but is your business friendly for the environment? Many companies use this approach to strengthen their brand awareness. However, there are businesses where sustainability...
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As global and more complex, pharmaceutical supply chains need a significantly more resilient business climate. Causes of origin Pharma supply chain is with complex character in the first place. But COVID-19 sparked more significant challenges, highlighting the need for companies to build a resilient supply chain. Starting...
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Track and trace among Food Supplements industry – the missing part in the fight against drug counterfeiting The track and trace of food supplements is a polarizing topic among the supply chain participants. Many moving pieces are on the road toward reaching unanimity and developing an...
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Egypt is working proactively on establishing a robust regulatory environment and already benefits from it. With USD 6.3 billion pharma market volume, Egypt is not only one of the biggest countries in Africa, but it is one of the fastest growing pharmaceutical markets. The largest producer...
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The document recommends using GS1’s EPCIS standard to provide and maintain electronic data. The issuing of these two draft guidances has a crucial role in Drug Supply Chain Security Act (DSCSA) Implementation. The intention is to be facilitated the creation of a uniform methodology for product...
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Africa, the second largest continent, is heading straight forward to a transparent and secure pharma supply chain. When we are talking about the establishment of regulatory requirements in the territory of a whole continent, the scenario is quite different and complicated for the supply chain participants....
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All terms regarding the regulatory harmonization in Africa that you need to know AMA African Medicines Agency AMRH African Medicines Regulatory Harmonization. The initiative that provide leadership in creating an enabling regulatory environment for pharmaceutical sector development in Africa AU African Union. It comprises five regions and has 55 members:...
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Business digitalization - significant goal and hidden benefits for the whole supply chain Everyone is talking about digitalization, investments in digital transformation, industry 4.0 and so on. However, this trend will continue its spread, gaining volume. The analysis shows that the importance of the digital market...
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