Ethic Medical Research Ltd.

Clinical Trials Regulatory Support

ETHIC Medical Research Ltd. guides our clients through the complexities of regulatory affairs with effective assessment and strategies to ensure a project progress quickly and efficiently.
Submission timelines and obtained approval letter based on local regulations in Turkey is determine after provide all necessary documents form client. ETHIC Medical Research Ltd. provide to client possible submission date and approval date.

• Final approval to carry out clinical research in The Ministry of Health,
• Approval in the regional committee for ethics,
• Obtaining permission of customs committee to import/export investigative product (IP), biological specimens and medical equipment,
• Translation services, including back translation.