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!
External link for ProPharma
Vote now in our poll and share your insights with industry leaders. Your input helps shape the future of PV services! Learn more: https://lnkd.in/eXQF6-b5.
This content isn’t available here
Access this content and more in the LinkedIn app
We’re excited to see you at the J.P. Morgan Healthcare Conference in San Francisco, California, next week! We’ve supported hundreds of companies in achieving successful regulatory meetings and submissions. We’re passionate about helping organizations navigate FDA and EMA product development, and we’d love to discuss how we can assist your team. If you’re interested in connecting, let’s schedule a time to meet. We look forward to sharing insights and exploring ways to collaborate! Jeff Antos
Are you headed to San Francisco for the J.P. Morgan Healthcare Conference? We want to meet with you. Throughout the week of January 13-16, our leadership team will attend JP Morgan and will be available to discuss how to move your product through drug development to regulatory approval, assure compliance with applicable FDA/EMA/global regulatory guidelines, and answer any questions you may have. Whether you are approaching your initial regulatory interactions, a marketing application, or commercial-stage lifecycle management and compliance, we can help. Contact us today to schedule a time to meet with our regulatory experts.
Navigating the complexities of REMS programs? ProPharma's journey is one of expertise, precision, and partnership. From design to implementation, our REMS support helps ensure patient safety and regulatory compliance every step of the way. Discover how we streamline the process, tackle challenges, and keep your programs on track: https://lnkd.in/eQDNZpMG.
Heading to the DIA Global Pharmacovigilance and Risk Management Strategies Conference 2025? Join ProPharma (Booth #111) at this premier event, where regulators and industry experts come together to discuss the latest updates, challenges, and strategies in drug safety. 📍 Location: Baltimore, MD 🗓️ Dates: January 27–29 Let’s connect! Schedule a meeting with us here: https://lnkd.in/eaFHe2Y2! We look forward to seeing you there! Jennifer Miller Heather Thompson
Celebrating Excellence at the 2024 The The National Institutes of Health Institutes of Health Clinical Center CEO Awards! We honor our exceptional colleague, Kevin Schipper, for his outstanding achievements at NIH's Clinical Center CEO Awards Ceremony. Your dedication and contributions drive meaningful change and inspire us all! Congratulations to each awardee – your hard work makes a lasting impact, and today we celebrate you! A special thank you to Dr. Gilman and the NIH Clinical Center for hosting this event and recognizing excellence across our community. Here’s to continued success and even greater accomplishments ahead! [In the photo, left to right: Pius Aiyelawo, SES, FACHE (Acting CEO), Kevin Schipper, Dr. David Lang (Chief, Office of Patient Safety and Clinical Quality). #NIHExcellence #LeadershipInAction #WeAreProPharma
Navigating the complexities of EU GMP compliance just got easier! Our blog explores the essential aspects of EU GMP (Good Manufacturing Practice) compliance, offering a comprehensive guide for companies navigating this regulatory landscape. Whether you're new to pharmaceutical manufacturing or an industry veteran, staying up-to-date with EU GMP guidelines is critical to ensure product quality, safety, and regulatory approval. Key takeaways: - Understanding EU GMP principles and their role in quality assurance - Practical steps to achieve compliance - How to maintain ongoing adherence in a fast-evolving market Ready to ensure your operations meet the highest standards? Learn more: https://lnkd.in/eM_EdHvv!
Received an FDA Form 483? The clock is ticking. You have just 15 days to respond and prevent further regulatory action. Our blog breaks down what to do when faced with a 483, how to craft an effective response, and strategies to stay compliant and avoid future findings. ✅ Don’t let those 15 days become 15 days of panic! https://lnkd.in/eAtuVpxa
Is your team keeping up with the evolution of the Benchling platform? New applications and enhanced module capabilities transform how you collaborate, centralize data, and make data-driven decisions. But are you fully leveraging these advances? We help you maximize your Benchling investment with strategic consulting, seamless implementation, and managed services. Let’s ensure your platform evolves at the speed of science. Learn more and get started here: https://lnkd.in/etGUdYdH #Benchling #DigitalTransformation
Heading to San Francisco for the JP Morgan Healthcare Conference? Let’s Connect! From January 13-16, our leadership team will be attending the JP Morgan Healthcare Conference and is eager to meet with you. Whether you’re navigating early regulatory interactions, preparing a marketing application, or managing commercial-stage lifecycle and compliance, we’re here to help. Let’s discuss how we can support your journey from drug development to regulatory approval while ensuring compliance with FDA, EMA, and global regulatory guidelines. Don’t miss the opportunity to connect with our regulatory experts. Contact us today to schedule a meeting!
Are you headed to San Francisco for the J.P. Morgan Healthcare Conference? We want to meet with you. Throughout the week of January 13-16, our leadership team will attend JP Morgan and will be available to discuss how to move your product through drug development to regulatory approval, assure compliance with applicable FDA/EMA/global regulatory guidelines, and answer any questions you may have. Whether you are approaching your initial regulatory interactions, a marketing application, or commercial-stage lifecycle management and compliance, we can help. Contact us today to schedule a time to meet with our regulatory experts.
A well-defined data strategy is the cornerstone of any successful data-driven organization. Our extensive industry knowledge makes us understand what it takes to become a data-driven business. From data governance to data analytics, our comprehensive approach ensures that your data strategy aligns with your business goals. We can help you identify key data assets, establish governance frameworks, and implement best practices for data management. Our Services Include: - Data governance frameworks - Data quality management - Advanced analytics Transform your data into actionable insights: https://lnkd.in/eksSnr-i.