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Monthly archives: January, 2023

  • Medicine shortage: actions taken in Estonia and EU

    Medicine shortage: actions taken in Estonia and EU

    Lately the shortage of medicines and health products has become an important topic everywhere around the world. Health professionals from European countries, as well as from Canada and US have been warning about potential medicine shortage. In the end of December such effect were clear in Estonia too when antipyretic syrups were nowhere to be found. At the same time doctors needed to find alternative treatments for patients in need for some specific antibiotics since they were also short in supply. Causes of shortages The supply chain disruption in pharmaceuticals is actually nothing unprecedented. However, the past few years have

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  • CMC in pharma

    CMC in pharma

    Chemistry, Manufacturing and Controls (CMC) is a critical component of the drug development process. CMC in pharma is responsible for ensuring that the drugs being developed are safe, effective and high-quality. What is CMC? CMC stands for Chemistry, Manufacturing and Controls. It’s a term used in pharma to refer to various procedures involved in developing, producing and testing pharmaceutical products. CMC also includes processes such as identification of raw materials used in production, establishing standards of quality control and specifications for finished products. Furthermore, product stability testing, verifying manufacturing methods and equipment used in production.  The main purpose of CMC

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  • Change of legal name – officially TBD Pharmatech

    Change of legal name – officially TBD Pharmatech

    On Friday, 13th of January 2023 the legal name of our company was changed to osaühing TBD Pharmatech. We started using the new name already in September 2022 as it was a big part of the whole rebranding process. Now we can fairly say that the rebranding is complete and TBD-Biodiscovery has officially become TBD Pharmatech. Here‘s an article in Meditsiiniuudised about the rebranding of TBD.

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  • GMP for APIs

    GMP for APIs

    Good Manufacturing Practice (GMP) is a set on important requirements of the drug manufacturing process. It is a system for ensuring that active pharmaceutical ingredients (APIs) are produced safely, consistently and in compliance with relevant regulatory standards. What is GMP? GMP stands for Good Manufacturing Practice and refers to a set of guidelines that must be followed when manufacturing APIs. These guidelines are designed to ensure that the production process meets a certain level of quality control, safety and consistency. They have been developed by regulatory bodies such as the U.S. Food and Drug Administration (FDA) and the European Medicines

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