Blog posts

dscsa serialization requirements

[Blog] DSCSA 2023 – what is coming?

Key areas of DSCSA`s new requirements   The announcement that FDA officially confirmed the DSCSA 2023 Interoperability Deadline is a hot topic. The new requirements affect different aspects of track and trace process and meantime challenge all supply chain participants. Now is the time to meet the...

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interoperability pharma

[Blog] Understand the meaning of “interoperability”

  Interoperability - the road towards Connected Healthcare   If you are in the pharma world, we are sure that you meet the word “interoperability” at least once a day. Definitely, this term became trendy, especially over the past year regarding the new DSCSA requirements. However, we should...

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brazil anvisa requirements deadline

[Blog] Brazil ANVISA Deadline is Official

28th April 2022 is the official deadline for meeting Track & Trace requirements as the Brazil Health Regulatory Agency (ANVISA) has approved its final Normative Instruction (NI 100). The date is set and all pharma supply chain participants have just 6 months from now to...

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cloud services challenges

[Blog] Challenges in front of cloud services

Key challenges in front of cloud services that you have to take into account   According to research in 2022, the global public cloud services market is expected to grow by approximately 22%, which amounts to about 482 billion U.S.D. Moreover, focusing on the pharma industry, the...

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[Whitepaper] UDI – from the Basics to the Benefits

  Get the most detailed information about UDI - everything that supply chain participants need to know! With the implementation of the Medical Devices Regulation (MDR), it became apparent that manufacturers should assign UDI to medical devices. This is intended to allow the identification and to improve the traceability...

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[Blog] Traceability systems – more than just Track & Trace

Organizations that start implementing traceability can begin to take advantage of the radically increased insight and control they have over how their products are manufactured and distributed. We have been already discussed the fundamental impact of traceability systems on the different industries and the various supply...

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master udi-di eudamed

[Blog] What does Master UDI-DI stand for?

Master UDI-DI - the new EU requirements in regard to medical devices     With the implementation of the Medical Devices Regulation (MDR), it became apparent that manufacturers should assign UDI to medical devices. This is intended to allow the identification and to improve the traceability of devices,...

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pharma industry zero carbon emissions

[Blog] Mission: Zero carbon emissions

The sustainable environment is a subject under consideration for all participants in the supply chain for a long time.   We outlined the key first “green steps” from the Pharma industry in our free whitepaper. They could be the beginning of the road towards environmentally friendly manufacturing...

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Pharma Serialization, Aggregation and Track and Trace Software by SoftGroup Top

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