Welcome to Appletree CI Poland sp.z o.o.

Appletree CI Group is an expert niche CRO (Contract Research Organization) and global regulatory affairs service provider. We are specialized in contract clinical research services in Europe and regulatory affairs support on a global level.

Services

• Multinational clinical trials phases I, II, III and IV
  • Design of protocol, CRF, eCRF
  • Regulatory procedures
  • Feasibility
  • Monitoring
• Project management and consulting
• Regulatory affairs consulting and services worldwide
  • Regulatory strategy, Scientific advice, Life cycle management
  • CMC writing
  • Guidance on medical device classification, CE marking
  • Investigational Medicinal Product Dossiers (IMPD)
• Medical writing
  • Clinical study protocols and reports
  • Patient information and patient informed consent forms
  • Investigator’s brochure
  • Pediatric Investigation Plan (PIP)
• Biostatistics and data management
  • Case number calculation
  • Statistical analysis plan
  • Data Management / Electronic Data Capture (EDC)
  • Biostatistical analysis and statistical report

Expertise

At Appletree CI Group we focus on what we know best. Throughout the years, we have been focusing on the four areas we have expert know-how in: Ophthalmology, medical devices, dermatology and pediatric procedures.

Company

We are present in 11 European countries and have approx. 30 employees. By having an in-depth understanding of local cultures and customs, as well as experience with national regulations we are able to facilitate your clinical development and regulatory projects.

For further information please visit our corporate website
www.appletree-cig.com