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🧪📊 Clinical Research Consulting Packages

🧪📊 Clinical Research Consulting Packages

Clinical research demands strict regulatory compliance, structured planning, and professional execution.

To address this, our consulting services are delivered in package-based, project-specific, and internationally compliant formats.

Our goal is to ensure:

✔ Full regulatory compliance

✔ Data integrity and quality

✔ Operational efficiency

✔ Sustainable and audit-ready clinical research processes

🟢 Clinical Research Starter Package

🎯 For individuals and teams entering clinical research Designed for those new to the field or seeking a structured overview of the process.

📌 Overview of clinical research processes

📌 Introduction to ICH-GCP principles

📌 Roles and responsibilities in clinical trials

📌 Initial risk and process assessment

👉 Message us for package details and pricing.

🔵 Clinical Research Pro Package

🧑‍⚕️ Operational support for ongoing clinical trials Ideal for active studies requiring professional operational guidance and CRA-focused support.

📌 Clinical trial operational consulting

📌 CRA processes and site management support

📌 GCP and regulatory compliance consulting

📌 Data integrity and quality control processes

📌 Documentation and reporting support

👉 Contact us to receive package scope and pricing information.

🟣 Clinical Research Advanced Package

🌍 For national and international clinical studies Tailored for Sponsors, CROs, and research teams managing multi-center or international trials.

📌 National and international regulatory compliance

📌 Ethics committee and regulatory process guidance

📌 Risk-based monitoring (RBM) and quality management

📌 Therapeutic area expertise (inc. Oncology & Cardiology)

📌 Process optimization and performance evaluation

👉 Project-based pricing available upon request.

🔴 VIP Clinical Research Consultancy

👑 End-to-end, high-level clinical research management Our most comprehensive service for organizations seeking full management and strategic oversight.

📌 End-to-end clinical trial consulting

📌 Strategic guidance for Sponsors and CROs

📌 Audit, inspection, and regulatory readiness support

📌 One-to-one support for critical trial phases

📌 Priority communication and dedicated follow-up

👉 Message us for VIP package details and customized pricing.

💳 Pricing Policy

📌 All clinical research consulting services are fee-based 💳.

📌 There is no fixed standard pricing.

📌 Fees are determined based on trial phase, scope, and duration.

📌 Each project receives a customized quotation.

📌 All services are delivered under strict confidentiality 🔒 and ICH-GCP ethical standards.

📲🚀 Get in Touch Today

🧪 Don't leave your clinical research to chance.

📊 Ensure regulatory compliance and data quality.

🏥 Strengthen your clinical trials with professional consulting.

👉 Send us a message now to receive package details and pricing information.

müşteri 1

Gökhan DAG,
Dag Mühendislik Kurucusu

Dag Engineering CEO'su Gökhan DAG Sayın GOKTAS ihtiyacımız olan çözümü hızlı ve etkili bir sekilde teslim etti. Profesyonel yaklasımları ve müsteri odaklı hizmetleri bizi gerçekten etkiledi. Onları şiddetle tavsiye ediyoruz!"

Melike Zeynep Çiftci – Klinik Araştırmacı

Melike Zeynep Çiftçi, Klinik Araştırmacı

Anıl GÖKTAS ile çalısmaktan büyük keyif aldım. Hızlı yanıt süreleri ve çözüm odaklı yaklasımları isimizi kolaylastırdı ve başarılı sonuçlar elde etmemizi sağladı."

Beyza Bayrak – Proje Asistanı

Beyza Bayrak, Proje Asistanı

Anıl GÖKTAS'ın sagladıgı hizmetlerden son derece memnun kaldık. Ekibin uzmanlıgı ve destefi sayesinde projelerimizi sorunsuz bir Sekilde tamamladık. Tesekkürler Anıl GOKTAS!"

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