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ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies. With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!
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Sharon Charles, Vice President of Clinical Operations, ProPharma, shared her expertise on our global consulting work and how she leads the Clinical Operations team within our Clinical Research arm. From guiding early-stage companies in bringing innovative therapeutics to market to integrating cutting-edge technologies like AI in drug development, Sharon highlighted how ProPharma is at the forefront of targeted therapies and cell & gene therapy. Her insights shed light on Australia's evolving clinical trials landscape and the #APAC region, particularly through our Gene Therapy Center of Excellence. Thank you, Sharon, for your valuable contributions to the future of clinical research! Watch the full interview! #RoadToTheMax #WeAreProPharma #GeneTherapy
We had an engaging conversation with Sharon Charles, VP of Clinical Operations at ProPharma Group, as part of Road to the Max: Australia. Sharon gave us an inside look at ProPharma’s global consulting work, where she leads the Clinical Operations team within their Clinical Research arm. From helping early-stage companies bring cutting-edge therapeutics to clinic and market, to integrating novel technologies like AI into drug development, Sharon shared how ProPharma is driving innovation in the targeted therapies and cell & gene therapy space. With the Gene Therapy Center of Excellence at the forefront, Sharon’s insights offered a comprehensive view of the expanding clinical trials landscape in Australia and the APAC region. Thank you, Sharon, for sharing your expertise on the exciting advances shaping the future of clinical research! Check out the full interview and the rest of the road trip: https://lnkd.in/eM8V73Ui Bethany Weller Scully | Suzan Leake | Benjamin Frey | Shu Lam | Rui Pereira | Nicole Santek | Jon Tuccillo | Amilcar Loureiro | Pavan Hemadri #roadtothemax #madmax #pharmaindustry #pharma #lifescience #biotech #clinicaltrials #australia #melbourne
We are excited to be Silver Partners and announce that Dr. Kiran Kandula, Senior Director of Pharmacovigilance at ProPharma, will speak at the 36th Pharmacovigilance India 202* conference, hosted by Virtue Insight! Join us from November 6th to 7th in Mumbai, where Dr. Kandula will contribute to the panel session on “Technology: Unlocking the Better Ways in Pharmacovigilance.” This is a fantastic opportunity to explore the evolving landscape of pharmacovigilance and how innovative technology is enhancing patient safety and compliance. 📅 Date: November 6-7, 2024 📍 Location: Hotel Kohinoor Continental, Mumbai, India 🔗 Register here: https://lnkd.in/ePM4u-zS We look forward to seeing you there!
We are delighted to announce our new speaker Dr. Kiran Kandula, Senior Director, Pharmacovigilance, ProPharma for Virtue Insight's #Pharmacovigilance India 2024 https://lnkd.in/gXgnQ2fC For our upcoming conferences visit : https://lnkd.in/gjQY86dn #VIphv #ClinicalSafety #patientsafety #RiskManagement #clinicaltrials #mumbai #clinicalresearch #pv #Qualitycontrol #pharma #healthcare #lifesciences #RegulatoryAffairs #RegulatoryWriting #MedicalWriting #scientificwriting #regulatory #medicinesaffairs #pharmaceuticals #biosimilars #biotech #patientcentric #vigilance #pharmaceuticalindustry
Transform your R&D processes with ProPharma's Benchling services! Our expertise in life sciences technology enhances collaboration, data management, and regulatory compliance. Discover how we can optimize your research workflows and drive innovation in your organization. Learn more about our Benchling solutions here: https://lnkd.in/etGUdYdH.
It’s Time to Prioritize Mental Health in the Workplace Mental health matters just as much as physical health. Let’s work together to build a supportive environment where well-being comes first—because a healthier mind leads to a stronger, more productive team. How do you prioritize mental health in your workplace? Share your tips or thoughts in the comments! 💬 #WorldMentalHealthDay #MentalHealthMatters
ProPharma has been awarded the 2024 CPHI Regulatory and Compliance Award! We’re proud to be recognized for our innovative approach to regulatory and compliance services in the life sciences industry. With our cutting-edge AI tools, we help our clients navigate complex regulatory landscapes, ensuring compliance and accelerating the delivery of life-saving therapies. “As a team, we’re dedicated to enhancing our ability to streamline critical activities,” said our CEO, Dawn Sherman. This award is a testament to our commitment to improving global health. Thank you, CPHI! https://lnkd.in/eKwtVs-D #WeAreProPharma #CPHI2024
Join ProPharma at the 2024 American Medical Writers Association (AMWA) Conference! We're excited to connect with industry leaders and share insights on enhancing communication in the medical field. Don’t miss this opportunity to learn, network, and advance your skills! Meet us at booth #23! Rachel Medal Janice Worley Katherine Wright, Ph.D. Makayla Manfull, PharmD CJ Glaser Simone Otto Krystin Hill Rajasi Joshi, PhD Connect with us: https://lnkd.in/e5shpz4Y #AMWA2024 #MedicalWriting
Periodic Safety Update Reports (PSURs) are essential for monitoring the safety and efficacy of medications post-approval. They analyze real-world data to uncover rare adverse reactions and ensure ongoing public health protection. Discover how PSURs evolved into Periodic Benefit-Risk Evaluation Reports (PBRERs) and their crucial role in safeguarding our health. Read more from Clinical Leader!
Stay ahead in drug safety by mastering the use of Periodic Safety Update Reports (PSURs) and their evolution into Periodic Benefit-Risk Evaluation Reports (PBRERs) to ensure ongoing public health protection. https://lnkd.in/en7gPHeF Source: ProPharma
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Join us at the European Society of Gene and Cell Therapy Congress. ProPharma and PBL will present the CF Box, a fully automated cell factory transforming Cell and gene Therapy (CAGT) manufacturing. This innovative device enhances flexibility, reduces costs, and supports advancements in therapy development. Visit Eleonora Casucci at booths E09 and E11 to learn how the CF Box is driving the future of CAGT! Learn more: https://lnkd.in/ej_TSUG4. Eleonora Casucci #ESGCT #CellGeneTherapy #WeAreProPharma