All Regulatory Services shall be conducted by our experienced specialists in Regulatory Affairs

• Dossier preparation and submission to the Turkish Medicines and Medical Devices Agency (TİTCK) and follow-up of procedures
• Start-Up Services
• Determining missing document for CTD applications (Gap Analyses)
• Determining missing document for CTD applications (Gap Analyses)
• Participating in teleconferences and video conferences where necessary to enable the flow of information for relevant projects
• Correspondence with the Ministry of Health
• Responding to letters regarding missing information
• Ensuring the lifecycle of the product