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The Latin American Pharmaceutical Market: Why Specialty Generics Are Poised for Growth As the pharmaceutical industry continues to evolve, one trend is becoming increasingly clear: the demand for specialty generics is on the rise, particularly in the Latin American market. But what exactly are specialty generics, and why are they gaining traction in this region?
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As many as 20% to 50% of clinical trials do not accrue participants at the site level, leading to wasted time and financial resources. This waste can be minimized by early selection of trials most likely to succeed. The protocol feasibility review process informs this selection by offering a way to evaluate logistical elements of a clinical trial before the activation process is started.
Speaker: Simran Kaur, Co-founder & CEO at Tattva.Health
AI is transforming clinical trials—accelerating drug discovery, optimizing patient recruitment, and improving data analysis. But its impact goes far beyond research. As AI-driven innovation reshapes the clinical trial process, it’s also influencing broader healthcare trends, from personalized medicine to patient outcomes. Join this new webinar featuring Simran Kaur for an insightful discussion on what all of this means for the future of healthcare!
Metsera, Inc., a clinical-stage biotech company focused on developing next-gen injectable and oral nutrient-stimulated hormone (NuSH) analog peptides for the treatment of obesity, overweight and related conditions, has priced its initial public offering (IPO) at $18.00 per share, raising $275 million in gross proceeds. Current Share Price: The offering, which includes 15,277,778 shares of common stock, is set to close on February 3, 2025, after beginning trading on the Nasdaq under the ticker sy
The FDA has paused a study of Amgen’s early-stage candidate AMG 513. Elsewhere, Valneva got another approval and a radiopharma developer raised $112 million.
In an increasingly competitive market, organizations involved in clinical trials or participant-driven research programs cannot afford to have a cumbersome or confusing recruitment and enrollment process. A seamless, efficient, and supportive experiencefrom first contact to trial participationcan make all the difference in attracting and retaining participants, ultimately ensuring the success of your trial.
Speaker: Simran Kaur, Founder & CEO at Tattva Health Inc.
The healthcare landscape is being revolutionized by AI and cutting-edge digital technologies, reshaping how patients receive care and interact with providers. In this webinar led by Simran Kaur, we will explore how AI-driven solutions are enhancing patient communication, improving care quality, and empowering preventive and predictive medicine. You'll also learn how AI is streamlining healthcare processes, helping providers offer more efficient, personalized care and enabling faster, data-driven
In this episode, Ayesha spoke with Mario Marcondes, MD, PhD, VP Head of Clinical Development at Nektar Therapeutics , a company focused on the discovery and development of novel therapies for autoimmune disorders and cancer. Dr. Marcondes is a licensed and trained physician, specializing in oncology and immune oncology. He has more than 15 years of research and teaching experience in Bone Marrow Transplant (BMT)/Cellular Therapies and more than 10 years of industry experience.
Integrating E-Clinical Technologies in smarter clinical trials improves efficiency, enhances data accuracy, and streamlines clinical research for better patient outcomes. With the increasing world population, clinical trials are now more […] The post The Role of Integrating E-Clinical Technologies In Smarter Clinical Trials appeared first on ProRelix Research.
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Emerging animal diseases Event type: symposium Audience: scientists Description: Sciensano organises together with the Federal Agency for the Safety of the Food Chain ( FASFC ), ARSIA and DGZ , the 10th symposium on animal health. The spoken language of this event is Dutch or French. Hence, more information about this course can be found on the Dutch or French version of the event page.
Contents About the Study Why Participate? Your Rights Who Can Participate? More Study Details About the Research Center Study Location Research Center: Baylor College of Medicine Location: 1977 Butler Blvd Houston Texas 77030 Lead Researcher: Sanjay J. Mathew, M.D. IRB: This study has been reviewed and approved by the Baylor College of Medicine Institutional Review Board About the Study Could brain imaging hold the key to more effective PTSD treatments?
Thank you to SCOPE Summit for recognizing Velocity at the 2025 Site Innovation Award presentation! Our presentation focused on the way VISION is enhancing trial accessibility for participants worldwide. Now available in four countries and four languages, the VISION Engage mobile app has been downloaded more than 100,000 times. To date, VISION has supported: 8,700 randomizations $5.3M in-app patient stipend payments Continuous data refinement on 1.5M patients Learn more about VISION > The
Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinical supply packaging facility in Shiga, Japan. Strategically located between Tokyo and Osaka, and one of largest in Japan, this 6,000 square meter facility offers comprehensive services including primary and secondary clinical packaging and labelling, comparator sourcing, cold chain storage, local and global distribution, local language support and white glove service to support stud
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