Discover the power of our global contact center! From multilingual support to 24/7 availability, we ensure seamless service worldwide, tailored to local cultures and regulatory standards. Empower your global outreach today: https://lnkd.in/ehwyeGVA!
ProPharma
Business Consulting and Services
Raleigh, North Carolina 125,321 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
-
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
-
Managing vendor audits efficiently while maintaining compliance can be challenging. Explore how outsourcing can streamline processes and maximize cost efficiency in our insightful blog: https://lnkd.in/eBXdTB-A.
-
Every marketing authorization holder (#MAH) needs a robust pharmacovigilance (#PV) system to ensure product safety. This system monitors the safety of medicinal products and detects any changes in their risk-benefit balance. Key components include the Qualified Person for Pharmacovigilance (#QPPV) and Local Persons responsible for Pharmacovigilance (#LPPV). Learn how to navigate the complexities of PV systems and meet regulatory requirements effectively. Read our blog to learn more: https://lnkd.in/e9K_MJnE.
-
Cast your vote in this week's poll about Medical Information (MI), and stay informed! https://lnkd.in/gkg-jXcA #ProPharmaPolls #PharmaInsights
This content isn’t available here
Access this content and more in the LinkedIn app
-
Happy World Social Media Day from ProPharma! 🌐✨ Join us in advancing life sciences through innovation and collaboration. If you're not already, follow us for the latest research, insights, and industry updates! Instagram: @propharma_global Facebook: ProPharma Twitter/X: @ProPharmaGroup #WorldSocialMediaDay #LifeSciences #WeAreProPharma
-
We are looking forward to seeing you today! If you haven't already, stop by our booth #104 at Future Labs Live Basel. Eliot Randle, Andy Newell, and Alex Butcher are waiting to tell you how ProPharma may be your best solution.
Come and visit the ProPharma booth (#104) at Future Labs Live Basel. Eliot Randle, Andy Newell and I look forward to welcoming you. #futurelabslive2024
-
-
Creating a highly efficient Promotional Review Committee (PRC) isn't just about having top-notch reviewers and best practices. It all begins with a well-prepared Medical, Legal, and Regulatory (MLR) submission. This often underrated step is crucial for a smooth PRC process, directly impacting review speed and efficiency. At ProPharma, we ensure your MLR submissions are best-in-class, setting up your PRC for success from the start. Whether you're new to the process or looking to enhance your current system, our expert consultants are here to help. Read more in our latest blog: https://lnkd.in/eFFNXCfR.
-
ProPharma simplifies access to Cell and Gene Therapies by offering empathetic, personalized support across every stage of the treatment journey. From financial navigation to emotional assistance, our comprehensive Patient Support Programs ensure patients can focus on what truly matters: their health. Discover how our dedicated case managers and global support network make complex treatments more accessible and successful. Read our blog to find out more: https://lnkd.in/egMgSVeA. #CAGT
-
Eleonora Casucci, Vice President of Quality & Compliance EU, ProPharma discusses ProPharma's groundbreaking innovations in Cell & Gene Therapies in her latest interview with Pharma Industrial India. The CF Box is a tool which enables pharma organizations, hospitals and even research centers to advance their research and development of innovative medicine to address unmet medical needs. The CF Box is designed to provide functionalities that are not present in today’s market, which in conjunction with the access to ProPharma wealth of expertise is a unique recipe to overcome the challenges faced by those who aim at developing new C&G Therapies. Our CAGT Center of Excellence (CoE) supports #CAGTmanufacturers globally, and the CF Box is a prime example of our efforts to automate processes, meet high GMP standards, and overcome automation and cell culture challenges. Read more in Eleonora’s interview with Pharma Industrial India: https://lnkd.in/dBZ7hrqv. #ClinicalTrials #WeAreProPharma
ProPharma, with its CAGT Center of Excellence (CoE) is actively supporting #CAGTmanufacturers across the globe, emphasizes Eleonora Casucci, Vice President of Quality & Compliance EU, ProPharma in her latest interaction with Aishwarya Saxena, Pharma Industrial India. #healthcare #PharmaIndustrialIndia