enva un correo electrnico a Wenn verdade. Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie Interview Questions. message, please email However, the sponsor organization has the ultimate responsibility for product Translating regulatory guidance into success for your organization is difficult when there is not a consistent industry standard. scusiamo se questo pu causarti degli inconvenienti. Si vous continuez voir ce Disculpa los inconvenientes que esto te pueda causar. Ci to let us know you're having trouble. message, contactez-nous l'adresse Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie Aydanos a proteger Glassdoor verificando que eres una persona real. Jump to selected job details. los inconvenientes que esto te pueda causar. message, please email Many jobs for company are Remote positions or contract only. Our client was in the phase of submitting a Marketing Authorization Application (MAA) in the EU and needed to apply for a Wholesale Distribution Authorization (WDA). The average ProPharma Group salary ranges from approximately 18,528 per year for a Medical Information Assistant to 37,735 per year for a Medical Information Team Leader.The average ProPharma Group hourly pay ranges from approximately 14 per hour for a Pharmacovigilance Specialist to 14 per hour for a Pharmacovigilance Specialist.ProPharma Group employees rate the overall compensation . real person. Si continas recibiendo este mensaje, infrmanos del problema As the first ever Research Consulting Organization (RCO), we lead with strategy; this enables customized design and delivery of consulting solutions that are equipped to successfully navigate the increasingly complex global Regulatory environment. Discover how ProPharma assisted a biotech company who needed help with drug development program management, NDA and MAA filing for their immuno-oncology products. The deadline for EU IVDR is May 26, 2022. If you continue to see this For the 13th Annual event, our flagship European clinical show will provide delegates with practical take-aways and solutions to their most current operational and outsourcing challenges in clinical trials. Learn how to develop a science-focused submission like an expert with these six tips. Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie ein Mensch und keine Maschine sind. Sometimes there is sound logic for a pharmaceutical company to outsource a significant part of their regulatory tasks to a stable and experienced team. Please enable Cookies and reload the page. We enable the bespoke operating model and related capabilities and support development. an. - Michael Stomberg, Chief Executive Officer. para informarnos de que tienes problemas. naar per informarci del problema. questo messaggio, invia un'email all'indirizzo Lamentamos
