ProPharma

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!

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.

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

Great event this morning to see ProPharma named in the Top 100 businesses in North Yorkshire! Thanks to The Press and York St John University

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.

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