Several crucial challenges of track and trace project implementation in 2021 The track and trace solutions market is projected to reach USD 4.21 billion by 2024 from USD 2.16 billion in 2019, at a CAGR of 14.2%. Factors such as the stringent regulations & standards for...
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Updated: 5th March 2021 In fact, this is jargon from the highly technical field of supply chain management. But what actually is included in the L1-L5 serialization solutions? Here is the simplest explanation with less jargon. Moreover, what makes SoftGroup the best choice for all your...
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Pharma Aggregation is a new opportunity in Supply Chain drug traceability. It has been considered as the next logical step after serialization by the industry expert, especially when the single package serialization is identified as proofed protection against counterfeiting and drug integrity. The USA’s Drug Supply...
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Supply chain visibility becoming more important What is supply chain visibility? A common definition of supply chain visibility is the ability to track raw materials and components from original suppliers and manufacturers through the organization’s manufacturing facilities to customers. To gain benefits from this, such supply chain...
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Currently, the UK is a participant in the European regulatory network for medical devices, but after the end of the transition period, this participation will also end. The Medicines and Healthcare products Regulatory Agency will take on the responsibilities for the UK market undertaken through...
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The EU's Medical Device Regulation (MDR) was officially published on 5 May 2017 and came into force on 25 May 2017. The MDR will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC). In this whitepaper, you...
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Thanks to the research of the European Pharmaceutical Review, we are witnessing a wide examination of how the pharmaceutical supply chain is faring in the face of growing concerns about the impact of a sudden market disruption on the quality and availability of medicines. A...
Read More![[Glossary] EU MDR and IVDR: The core terms you should know](https://cdn.shortpixel.ai/client/q_glossy,ret_img,w_900,h_400/https://www.softgroup.eu/wp-content/uploads/2020/10/Untitled-design-38.png)
The European Union (EU) is approaching its deadline to implement the Medical Device Regulation (EU MDR). As the transition period ends on May 26, 2020, a wider and clearer regulatory scope for medical devices is just around the corner. The EU MDR establishes requirements for manufacturers...
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Last updated: 1st February 2021 Since the European medical device regulation is experiencing a major overhaul medical device manufacturers have to adjust their strategic approach to go through this change smoothly. The EU regulators take this action as an effective step towards enabling the Digitalization of...
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Download the whitepaper now by filling the fields below and learn about the UDI requirements around the world. [contact-form-7 id="8530" title="Contact form - Aggregation Medical devices_UDI requirements"]...
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