Adem Ali YILMAZ’s Post

A staggering $42 billion is wasted globally each year due to medication errors and that's not the most alarming part. What's truly concerning is that most of these errors are preventable! The World Health Organization data shows that over half of healthcare harm, particularly medication errors, can be avoided. At Tiga Healthcare Technologies, we prioritize patient safety and develop healthcare IT products with a systemic approach, minimizing inefficiencies and preventing errors at the root cause. In 2010, we developed the first of its kind, the Pharmaceutical Track & Trace System, branded as DrugXafe, to achieve a reliable pharmaceutical supply chain with an end-to-end system. This innovative system uses 2D Data Matrix codes to track and trace each single drug box from production lines all the way to patients. It currently operates in three countries in collaboration with ministries of health, drug regulatory bodies and a pharmaceutical supply chain network of over 65,000 stakeholders, such as pharmacies, consumption centers, manufacturers, wholesalers and reimbursement institutions. We innovate advanced healthcare IT technologies to empower safer medication use and prevent medication-caused healthcare errors, upholding the WHO's 'First, do not harm' principle for a healthier future. Let's shape the future together, as always! For further insights:  https://lnkd.in/d69gS5yC #Tiga #HealthcareIT #PharmaIT #DrugXafe #DrugTraceability 

𝗪𝗼𝗿𝗿𝗶𝗲𝗱 𝗮𝗯𝗼𝘂𝘁 𝘁𝗵𝗲 𝘀𝘁𝗮𝗯𝗶𝗹𝗶𝘁𝘆 𝗮𝗻𝗱 𝘂𝘀𝗮𝗯𝗶𝗹𝗶𝘁𝘆 𝗼𝗳 𝘆𝗼𝘂𝗿 𝗱𝗿𝘂𝗴 𝗽𝗿𝗼𝗱𝘂𝗰𝘁? At ten23 health, your full-integrated CDMO for sterile drug products, our 𝗳𝗼𝗿𝗺𝘂𝗹𝗮𝘁𝗶𝗼𝗻 𝗱𝗲𝘃𝗲𝗹𝗼𝗽𝗺𝗲𝗻𝘁 𝗲𝘅𝗽𝗲𝗿𝘁𝘀 ensure that your product is not only stable and effective but also efficiently prepared for clinical and commercial success and usability. We ensure timely delivery and can anticipate and de-risk potential development issues. 𝗧𝗶𝗿𝗲𝗱 𝗼𝗳 𝘁𝗮𝗹𝗸𝗶𝗻𝗴 𝘁𝗼 𝗖𝗗𝗠𝗢𝘀 𝘁𝗵𝗮𝘁 𝗱𝗼𝗻'𝘁 𝘁𝗵𝗶𝗻𝗸 𝘁𝗵𝗿𝗼𝘂𝗴𝗵 𝘁𝗵𝗲 𝗲𝗻𝘁𝗶𝗿𝗲 𝗱𝗿𝘂𝗴 𝗺𝗮𝗻𝘂𝗳𝗮𝗰𝘁𝘂𝗿𝗶𝗻𝗴 𝗽𝗿𝗼𝗰𝗲𝘀𝘀? We get it. At ten23 health, we take a holistic approach to 𝘀𝘁𝗲𝗿𝗶𝗹𝗲 𝗽𝗿𝗼𝗱𝘂𝗰𝘁𝘀, from formulation to primary packaging to device, from process unit operations and ranges to GMP filling. From pre-clinical through clinical to commercial stages, our integrated services ensure that every step of your drug product’s journey is executed with precision and foresight. 𝗖𝗼𝗻𝗰𝗲𝗿𝗻𝗲𝗱 𝗮𝗯𝗼𝘂𝘁 𝗾𝘂𝗮𝗹𝗶𝘁𝘆, 𝘆𝗶𝗲𝗹𝗱 𝗮𝗻𝗱 𝘁𝗲𝗰𝗵𝗻𝗶𝗰𝗮𝗹 𝘀𝘂𝗰𝗰𝗲𝘀𝘀 𝗼𝗳 𝘆𝗼𝘂𝗿 𝘀𝘁𝗲𝗿𝗶𝗹𝗲 𝗱𝗼𝘀𝗮𝗴𝗲 𝗳𝗼𝗿𝗺𝘀? You don’t have to be. Our advanced solutions - integrating formulation development, sterile fill & finish and testing - are designed to meet the highest standards, ensuring your product is of right quality, best yield and technically de-risked. 𝗟𝗼𝗼𝗸𝗶𝗻𝗴 𝗳𝗼𝗿 𝗮 𝗖𝗗𝗠𝗢 𝘁𝗵𝗮𝘁 𝗳𝗲𝗲𝗹𝘀 𝗹𝗶𝗸𝗲 𝗮𝗻 𝗲𝘅𝘁𝗲𝗻𝘀𝗶𝗼𝗻 𝗼𝗳 𝘆𝗼𝘂𝗿 𝘁𝗲𝗮𝗺? At ten23 health, we believe in true partnership. Our team of seasoned professionals works alongside you to ensure seamless project execution, from concept to patient delivery. We don’t just offer services—we provide solutions that drive your product forward. 𝗪𝗼𝗻𝗱𝗲𝗿𝗶𝗻𝗴 𝗵𝗼𝘄 𝘆𝗼𝘂𝗿 𝗖𝗗𝗠𝗢 𝗰𝗮𝗻 𝗮𝗹𝗶𝗴𝗻 𝘄𝗶𝘁𝗵 𝘆𝗼𝘂𝗿 𝘀𝘂𝘀𝘁𝗮𝗶𝗻𝗮𝗯𝗶𝗹𝗶𝘁𝘆 𝗴𝗼𝗮𝗹𝘀? As the 𝗳𝗶𝗿𝘀𝘁 𝗕-𝗖𝗼𝗿𝗽 𝗰𝗲𝗿𝘁𝗶𝗳𝗶𝗲𝗱 𝗖𝗗𝗠𝗢, ten23 health is committed to not only delivering quality pharmaceutical products but doing so in a way that’s socially and environmentally responsible. We incorporate sustainable practices throughout the drug development process, ensuring you can meet both your business and environmental objectives. 𝗬𝗼𝘂𝗿 𝘀𝘂𝗰𝗰𝗲𝘀𝘀 𝗶𝘀 𝗼𝘂𝗿 𝗺𝗶𝘀𝘀𝗶𝗼𝗻. Let’s discuss how we can deliver your sterile drug product with confidence, speed, and sustainability: 𝗮𝘁 𝘁𝗵𝗶𝘀 𝘂𝗽𝗰𝗼𝗺𝗶𝗻𝗴 𝗖𝗣𝗛𝗜 if you happen to be in Milan, or contact us via e-mail: contact@ten23.health Find out more on our services here: www.ten23.health #ten23health #pharma #CDMO #FormulationDevelopment #SterileManufacturing #fillfinish #DrugSafety #PharmaInnovation #GMP #LifeSciences #Sustainability #BCorp #CPHI #Milan

The introduction of the international recognition procedures by the MHRA represents a significant advancement in the accessibility of biosimilars within the UK. The IRP streamlines the approval process for biosimilars that have already been authorized by specified regulators. This means that biosimilars approved in these regions can now be automatically available without the need for additional clinical efficacy testing or bridging studies, thereby expediting patient access to these vital treatments. This not only benefits patients in the UK but also promotes consistency and collaboration among regulatory agencies worldwide. #Biosimilars #Healthcare #Regulation #BioTech

Learn from our amazing panellists Prasad Satam, Lokesh Patel, RAMAKRISHNA BOLISETI, Prashant Kumar Gupta, Balaram Patro, Sekhar Babu Puli, Uttam chakravarty as they will discuss about Packaging & Labelling: Playing with innovations & latest developments in Serialization, Track & Trace – Fight against the FAKES in #Pharma #Packaging,  #Labelling, #Serialisation, Track & Trace, #SupplyChain 2024 https://lnkd.in/getgsZsv For our upcoming conferences visit : https://lnkd.in/gjQY86dn #VIpplst #TrackTrace #Traceability #Anticounterfeiting #smartpackaging #packaginginnovation #pharmalabelling #artwork #pharmalabels #scm #anticounterfeit #barcode #Counterfeit #Healthcare #medicines #Drugregulatory #Pharmaceuticals #clinicaltrials

Is your drug safe and effective? 💉 ▶️Our focus today: Dose Administration, Compatibility & Usability.◀️ 🟣How do you ensure your drug product is designed for safe and effective administration to the patient? 🟣Do you account for variations in drug delivery and use across different settings? 🟣How do you evaluate drug product stability and quality during administration? 🟡Are you confident your administration procedures deliver the correct dose to patients while guaranteeing efficacy and safety at all times? 🟡Do you consider or are requested using a Closed-System-Transfer Device (CSTD), but are unsure about its impact on dose and product quality? When it comes to the development and manufacturing of sterile drug products, there is too much at stake to compromise on quality and safety- and you need to make the right choices. At ten23 health, we support our clients in taking the right decisions. We are specialists in developing sterile drug products that are not only effective but that can also be safely administered. We design tailored strategies from pre-clinical through commercialization, ensuring optimal usability for both patients and healthcare professionals. Our rigorous testing includes simulated administration experiments to guarantee product quality and stability - at all times. Curious to learn more about how we can enhance your drug product delivery and usability? Explore our services here: https://lnkd.in/dzv85Yvy #ten23health #services #drugdelivery #cdmo #pharma #DrugDevelopment #PatientSafety

🧬𝗕𝗶𝗴 𝗡𝗲𝘄𝘀 𝗳𝗼𝗿 𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗶𝗲𝘀!💊 TGA has updated labeling requirements for paracetamol-containing medicines. These updates include labeling exemptions that allow certain products to be labeled as "Pharmacy Medicine" instead of "Pharmacists Only Medicine." These changes are designed to help pharmacies adapt to new scheduling regulations while maintaining compliance. To understand how these adjustments impact the industry, read more in our latest blog 🔗 https://lnkd.in/dE7-aDZU www.arqon.com & www.attopolis.com May Ng ARQon l Asia Regulatory and Quality Consultancy | Deepak Jamle | ATTOPOLIS@ARQon-Asia Regulatory & Quality Consultancy (MedTech & Drug) #RegulatoryCompliance #ARQonGroup #AttopolisB2B2C #TGAUpdates #Paracetamol #LabellingExemptions #Medicines #PharmaIndustry #HealthcareInnovations #CollaborationInSingapore #MedTech

Increasing medication adherence rates is a global challenge for the consumer healthcare and the pharmaceutical industries. If people took their medication correctly, they’d get better, faster. So why is it so hard to make it happen in reality? Read this case study, in the Consumer Health Hub, to understand how Innovia Technology helped our client to get a step ahead by identifying actions to improve patient medication adherence. https://lnkd.in/ey2fbgJ9 #ConsumerHealth #Medication #Behaviour

The Uniform Code for Pharmaceutical Marketing Practices (UCPMP) 2024 was issued by the Department of Pharmaceuticals on March 13, 2024. The code governs the conduct of pharmaceutical companies in their marketing practices. It covers a number of aspects, including: Medical representatives Textual and audio-visual promotional materials Samples Gifts . #USCPMP #indianpharma #pharmaceutical #pharmamarketing

What Can The Pharma Industry Do To Tackle Fake Medicines? In a world where counterfeit medicines increasingly endanger public health, what pivotal actions can the pharmaceutical sector take to confront this crisis? Dive into the final episode of PharmTalks, where we examine the concerted strategies and cutting-edge solutions at play within the industry. The sophistication of counterfeit medications necessitates advanced and multifaceted counteractions, and knowing what to do is the first step! #counterfeitmedicine #fake #medicine #indianpharma #mrmed #trending #awareness

🌟 Celebrating National Brand Day – Proqlea Ltd.'s Commitment to Excellence 🌟 On National Brand Day, we take a moment to reflect on what makes the Proqlea Ltd. brand stand out in the pharmaceutical and clinical trial industry. At Proqlea Ltd., our commitment to quality 🏆, trust 🤝, and innovation 💡 shapes everything we do, and it’s the foundation of every service we provide. We’re proud to be a partner for businesses, offering timely delivery, regulatory compliance ✅, and transparency 🔍 in everything from clinical trials 🧪 to data management 📊. With a focus on patient rights and scalability, we build long-term relationships and help our clients navigate the ever-evolving pharmaceutical landscape. As a trusted partner, we prioritize efficiency and collaboration, working with renowned organizations to ensure the best outcomes. Our team of dedicated professionals strives for excellence and aims to exceed expectations every step of the way. Today, we celebrate the strength of the Proqlea brand and the values that have guided us to this point. Here’s to many more years of success 🎯, growth 🌱, and impact 💥! What makes your brand unique? Share with us how you’re making an impact in your industry! 💬 #NationalBrandDay #Proqlea #Quality #Trust #Innovation #PharmaceuticalExcellence #Healthcare #BrandImpact #PatientRights #ClinicalTrials #Growth