Our Clinical Research Solutions are designed to streamline every phase of your clinical trials, from planning and execution to regulatory support. With a team of industry experts and innovative technology, we ensure your research moves forward efficiently while meeting the highest standards of compliance and quality. Let us be the partner you trust to bring your vision to life and accelerate breakthroughs in healthcare. Learn more about our CRS Service: https://lnkd.in/g_tg8ZyM
ProPharma
Business Consulting and Services
Raleigh, North Carolina 132,998 followers
End-to-end bespoke solutions that de-risk & accelerate our partners' and sponsors' drug and device development programs
About us
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!
- Website
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http://www.propharmagroup.com
External link for ProPharma
- Industry
- Business Consulting and Services
- Company size
- 5,001-10,000 employees
- Headquarters
- Raleigh, North Carolina
- Type
- Privately Held
- Founded
- 2001
- Specialties
- Compliance & Quality Assurance, Commissioning & Qualification, Product Lifecycle Management, Medical Information, Pharmacovigilance, Computer Systems Validation, Process Validation, Cleaning Validation, Technology Transfer, CMO Selection, Process Optimization, Clinical Safety, Regulatory Affairs, PAI Readiness, biopharmaceutical, Life sciences, and regulatory
Locations
Employees at ProPharma
Updates
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ProPharma has been named a finalist for Fierce Biotech CRO's 2024 Awards, with Matthew Weinberg, President of Regulatory Sciences, ProPharma recognized in the Leadership in Regulatory Compliance category! Our Regulatory Sciences team is dedicated to guiding clients through complex global regulations, ensuring quality and compliance at every step. This nomination underscores our commitment to excellence and innovation in regulatory support, helping our partners bring safe and effective therapies to market faster. Learn more about our Regulatory Sciences services: https://lnkd.in/ewZ25vEH. #WeAreProPharma
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Don’t Miss Out! Our Upcoming Webinar is Just 2 Weeks Away! Join us on November 19th for an insightful session, "Bridging from Clinical Development to Commercialization: Supporting Patients." Discover essential strategies and solutions for seamlessly moving from clinical development to commercialization, with a strong focus on patient support every step of the way. Whether you work on regulatory, clinical, or commercial teams, this webinar is designed to provide actionable insights that drive successful, patient-centered transitions in product development. Secure your spot today: https://lnkd.in/e9txrWdg. Eric Brandon, MBA, Director, Patient Services & Contact Center Operations Stephanie Pruett, Associate Director, Medical Information
Ready to enhance your understanding on how to support patients from the drug development process to commercialization? In our upcoming webinar, "Bridging from Clinical Development to Commercialization: Supporting Patients," we will discuss key strategies for ensuring patient support throughout the process. Don’t miss the chance to learn from Eric Brandon, MBA, Director, Patient Services & Contact Center Operations, ProPharma Stephanie Pruett, Senior Medical Information Manager, ProPharma, and elevate your approach to patient care. Secure your spot now for our November 19th webinar & Register here: https://lnkd.in/e9txrWdg. #PatientSupport #WeAreProPharma
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Time is running out! With the EU Clinical Trials Regulation (CTR) deadline approaching, sponsors face increasing pressure to ensure compliance. The new regulation transforms how trials are conducted across Europe, making it crucial to understand the changes and prepare effectively. Are you ready to adapt to the streamlined submission process, stricter timelines, and enhanced safety requirements? Discover the key steps to ensure your trials stay on track under the EU CTR: https://lnkd.in/eQZjKtG7)
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Come see us at the PV Virtue Insight Summit! #WeAreProPharma
Excited to be attending the 36th Pharmacovigilance (PV) VirtueInsight Summit! As Director of Business Operations at Propharma, I'm thrilled to share that we're a proud Silver Sponsor of this esteemed event. Day 1 has been fantastic, interacting with pharmaceutical industry stakeholders from Pharmacovigilance, Medical Information, Regulatory Affairs, Global Clinical Quality Management Systems, and more! Great insights from the experts of the industry and more to learn from the two day event, A R M Rao Dr.Hanumanthu Penchalaiah Mpharm PhD Sakshi Shrivastava Desai Dr. Rohini Pandey Dr Anuja Jawale (Sawant) Dr. Shraddha Bhange Renuka Neogi Dr. Aswin Kumar Dr. Sourabh Fulmali Indu Nambiar Dr. Kiran Kandula Dr. Kavita Lamror Dr. Mayur Maybhate @pratik shah Dr Santosh Taur, MD, DM, CMD Dr. Kushal Sarda Shiraz Kandawalla Sanjay Menon Jyoti Kashid Join us at our booth inside the Emerald II Conference Hall, Kohinoor Continental Mumbai, and let's connect! Malay Bhattacharjee Pavan Hemadri Dr. Amol Yelgaonkar Pinky Sharma Ankur Joshi Looking forward to another day of insightful discussions, networking, and collaboration. #WeArePropharma #Pharmacovigilance #PVSummit #Virtueinsight #SilverSponsor #Healthcare #PharmaceuticalIndustry #Networking #Mumbai #KohinoorContinental"
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Our team is eager to meet you at the Biomanufacturing World Summit in San Diego from November 19 to 21! Schedule a meeting with our experts— Tom Hunter, Allison Kazlauskas, Robert Beall, PMP, and Simona Mills, to discuss regulatory compliance, quality solutions, and collaboration opportunities. Stop by booth #35, and don't miss this chance to gain valuable insights! #BMWS2024
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Tap into this week's #ProPharmaPoll on our RDIT Solutions. Explore our services: https://lnkd.in/gVn7YVtg. #PharmaInsights
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Discover how ProPharma partnered with a leading global corporation to address increased product quality complaints and financial pressures. By implementing a tiered support system and leveraging offshore teams in India and the Philippines, ProPharma boosted operational capacity, controlled costs, and upheld high standards—ultimately expanding the engagement and showcasing the program’s outstanding success. Interested in the full story? Complete the form to download the case study instantly: https://lnkd.in/eq-BuPTH.
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Our team had an incredible time engaging with industry leaders, partners, and potential collaborators, sharing insights and exploring the future of pharmacovigilance together at World Drug Safety Congress Americas. One standout moment? A thought-provoking roundtable led by Angie R., Director of Systems & Submissions, ProPharma tackling the question: “Can AI replace humans within PV?” With a fantastic turnout, we’re thrilled to see the high interest in such a critical topic. A big thank you to everyone who joined us and contributed to the conversation! #WeAreProPharma
Business Development Manager at ProPharma Group | Medical Affairs | Medical Information | Post-Market Pharmacovigilance | Commercialization
We had a fantastic time at the World Drug Safety Congress Americas in Boston, connecting with current partners and meeting potential new collaborators to share our capabilities. A highlight was attending a roundtable hosted by our Director of Systems & Submissions, Angie Robertson. on "Can AI replace humans within PV?" The attendance for her talk was fantastic, and we extend our gratitude to all who joined. Laura Hopper Heather Thompson ProPharma #pharmacovigilance #Boston
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Navigating the Twists and Turns of FDA Approvals FDA Pre-Market Approvals (PMAs) can sometimes feel like a haunted maze. Our blog offers clear, strategic insights to illuminate your path—from submission best practices to proactively addressing potential concerns. These essential strategies can make your PMA journey far less daunting. Don’t let uncertainties lurk in the shadows—prepare and communicate effectively with the FDA. Explore the full blog here: https://lnkd.in/e5p5cete
The Care and Feeding of FDA PMAs: Mastering Premarket Approval
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