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IPHARMA / ChemDiv
IPHARMA / ChemDiv
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Medical Affairs *
Scientific Communications Development
Strategic Stakeholder Engagement
Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
Regulatory *
Labeling & Promotions
Maintenance & Renewals
Compliance
Transparency & Disclosure
Commercialization *
Customer Engagement
Brand Planning & Activation
Market Access & Policy *
Government Policy
Global Market Access
Pharmacovigilance *
Safety Systems
Risk Management
Finance & Investment *
Financial Services
Investment Banking
Quality & Mfg *
Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
Product Development
Trial Design & Planning
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Early Development
Digital Health Solutions
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Informatics Infrastructure
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7250 Parkway Drive, Suite 405, Hanover, MD 21076, USA
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IPHARMA / ChemDiv
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Accelerating Clinical Trials in Russia and the EAEU
ИФАРМА is a full-service contract research organization specializing in running efficient clinical trials and registering drugs and medical devices in Russia and the Eurasian Economic Union. With over 20 years of experience, they provide expertise in study startup, patient recruitment, regulatory compliance, and data management. Their services include feasibility studies, site selection and management, eCRF development, pharmacovigilance, and more.ИФАРМА's team includes over 150 experts dedicated to ensuring the highest quality standards and timely execution. They have conducted over 180 trials across 50+ indications, recruiting over 6,500 patients at more than 100 sites. Let ИФАРМА accelerate your clinical development in Russia and the EAEU.
Accelerating Clinical Trials in Russia and the EAEU
ИФАРМА is a full-service contract research organization specializing in running efficient clinical trials and registering drugs and medical devices in Russia and the Eurasian Economic Union. With over 20 years of experience, they provide expertise in study startup, patient recruitment, regulatory compliance, and data management. Their services include feasibility studies, site selection and management, eCRF development, pharmacovigilance, and more.ИФАРМА's team includes over 150 experts dedicated to ensuring the highest quality standards and timely execution. They have conducted over 180 trials across 50+ indications, recruiting over 6,500 patients at more than 100 sites. Let ИФАРМА accelerate your clinical development in Russia and the EAEU.
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7250 Parkway Drive, Suite 405, Hanover, MD 21076, USA
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