At LifeTech Staffing, we bridge talent and opportunity in the Life Sciences industry. Our commitment to excellence, personalized service, and strategic decision-making drives our success. Partnering closely with Medical, Pharmaceutical, and Biotechnology clients, we address staffing needs proactively. Whether you need specialized Quality Systems candidates or seek Regulatory, Validation, or Automation support, LifeTech Staffing is your trusted partner. Let’s build a stronger, more innovative future together
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The final quarter of 2024 will see some pivotal FDA decisions that could shape the biopharma landscape. #FDA #biopharma #drugapproval #lifesciences #healthcare
?? Seaport Therapeutics Launches with $100M to Advance Psychiatric Treatment ?? Exciting news in the biotech world! Seaport Therapeutics, a new venture out of PureTech Health, just secured $100M in Series A funding. The company aims to transform psychiatric treatment by developing cutting-edge therapies for mental health disorders. Seaport's approach is inspired by Karuna Therapeutics' successful journey with schizophrenia treatments, with hopes to address significant unmet needs in neuropsychiatry. With a talented team and growing investor interest, Seaport is set to make waves in mental health innovation. ?? #Biotech #MentalHealth #LifeSciences #VentureCapital #Neuropsychiatry Source: https://rb.gy/wdgq90
?? Novo Nordisk's Oral Rybelsus Shows Promise in Reducing Heart Disease Risks for Type 2 Diabetes Patients ?? Novo Nordisk's oral semaglutide (Rybelsus) has demonstrated significant potential in lowering cardiovascular risks in Type 2 diabetes patients, including reducing the likelihood of heart attacks and strokes. This advancement may pave the way for expanded approvals, offering an alternative to injectable treatments like Ozempic. The development is a testament to ongoing innovations in life sciences aimed at improving patient outcomes. Source: https://rb.gy/76834h #NovoNordisk #DiabetesCare #CardiovascularHealth #Rybelsus #LifeSciences #PharmaNews #MedicalInnovation #HeartHealth
Gilead Sciences is pulling Trodelvy's accelerated approval for treating bladder cancer after a phase 3 trial failed to show a significant survival advantage over chemotherapy. The study not only showed limited benefit but also reported a higher rate of treatment-related deaths, mainly linked to neutropenia. This follows previous setbacks for Trodelvy in other cancer trials, adding pressure on Gilead's oncology ambitions as it competes with rivals advancing in the antibody-drug conjugate space. Trodelvy's withdrawal reflects the complexities and setbacks in drug development, particularly in oncology, which can influence hiring demands for clinical trial specialists, regulatory experts, and research scientists. As companies like Gilead pivot their strategies, there may be shifts in workforce requirements, presenting opportunities for staffing firms like LifeTech to support talent needs in areas like clinical research, drug safety, and oncology-focused roles. https://rb.gy/uryig1 #Gilead #Trodelvy #CancerTreatment #PharmaNews #Oncology
?? Retention Matters in Staffing ?? At LifeTech Staffing, we believe the value of a placement isn’t just in finding the right talent—it’s in ensuring they stay long-term. The cost of employee turnover is staggering: replacing an employee can cost a company up to 2x their annual salary when factoring in recruitment, training, and lost productivity. That’s why we work overtime to ensure you are connected to the perfect position at the right company. Want to improve retention? Focus on the right fit, not just filling the role! #StaffingSolutions #TalentAcquisition #LifeSciencesJobs #AIJobs #WorkCulture (Source: ApolloTechnical, 2024)
Bristol Myers Squibb's $14 billion acquisition of Karuna Therapeutics is paying off with the approval of Cobenfy, a novel schizophrenia drug. This marks a significant breakthrough for an underserved condition that has seen little innovation in recent decades. Cobenfy, powered by KarXT technology, offers promising clinical performance with fewer side effects, addressing significant gaps in existing treatments like drowsiness and weight gain. This approval not only strengthens Bristol's neurology portfolio but also has the potential to reshape the treatment landscape for schizophrenia. The company is already exploring additional indications, including Alzheimer's-related psychosis and bipolar disorder. This exploration underscores a strategic investment in innovative solutions for chronic conditions. #PharmaInnovation #SchizophreniaTreatment #Neurology #LifeSciences #Biotech Source: https://rb.gy/xj2nzu
FluMist: AstraZeneca's First FDA-Approved Self-Administered Flu Vaccine After receiving FDA approval, AstraZeneca's FluMist has become the first self-administered flu vaccine. This nasal spray vaccine can now be used by adults aged 18-49 or administered by a caregiver to children aged 2-17. The move aims to increase convenience and accessibility, offering an alternative to traditional injections. FluMist, which contains weakened influenza virus strains, was first approved in 2003. The new approval adds flexibility in how people can protect themselves from the flu. However, a prescription is still required for purchase. #FluVaccine #FDA #PublicHealth #MedicalAdvances #HealthTech
?? FDA Draft Guidance: Integrating RCTs into Routine Clinical Practice?? The FDA's latest draft guidance aims to streamline randomized controlled trials (RCTs), integrating them into everyday clinical practice. Key points: ?? Utilize real-world data (RWD) from routine healthcare visits. ?? Simplify trial protocols for better patient access and faster enrollment. ?? Ensure data privacy and rigorous safety monitoring. ?? Encourage collaboration between healthcare providers and trial investigators. These changes could accelerate drug development, reduce costs, and yield more generalizable results, benefiting patients and the healthcare system. #ClinicalTrials #Biopharma #FDA #LifeSciences
The FDA has announced a new investigation into the potential contamination of tampons and other menstrual products with harmful metals, including lead, arsenic, and mercury. This inquiry stems from growing public concern over the safety of everyday personal care products, especially those used internally, which may expose individuals to dangerous substances over prolonged periods. The FDA’s review will focus on understanding how these metals may be present in menstrual products if they accumulate in the body and what potential health risks they pose. Despite the lack of widespread research on the subject, early data suggest that even low-level exposure to heavy metals can cause long-term health issues, such as reproductive harm, cancer, and other systemic effects. As these concerns gain visibility, the life sciences industry is tasked with innovating safer, more transparent product manufacturing and testing processes. LifeTech Staffing is at the forefront of placing professionals who drive advancements in health safety, compliance, and product innovation, ensuring that industry standards meet and exceed public expectations. We believe that talent plays a crucial role in ensuring the future of consumer safety in medtech and beyond. Read more at https://rb.gy/bf7ioo #LifeSciences #Biotech #FDA #HealthTech #ConsumerSafety #Innovation #Talent #Compliance #ProductSafety
?? **Breaking News in Lung Cancer Treatment** ?? Summit Therapeutics recently shared promising data regarding ivonescimab, a novel bispecific antibody, at the World Conference on Lung Cancer (WCLC). This drug, when combined with Keytruda (pembrolizumab), significantly improved progression-free survival for patients with advanced non-small cell lung cancer (NSCLC). The therapy demonstrated a potential to enhance immune response, offering hope for better outcomes in lung cancer treatments. As advancements like this emerge, LifeTech Staffing is committed to supporting the talent fueling these innovations. Get the full story at https://rb.gy/hkbbza #LungCancerAwareness #Biotech #LifeSciences #HealthcareInnovation #LifeTechStaffing