Apply directly via LinkedIn or send your resume to info@insight-cro.com
Insight - CRO
العيادات الطبية
Mohandiseen، Giza ٧٬٤٦٥ متابع
Clinical Research & PV Service Provider, Helping You To Achieve More Everyday | Let's Connect!
نبذة عنا
Insight Contract Research Organization (CRO) is a leading pharmaceutical service provider, offering comprehensive solutions in clinical research, pharmacovigilance, training, and regulatory affairs. With a focus on collaboration and integrity, we aim to exceed client expectations and drive meaningful progress in drug development, making a positive impact on patient's lives. For more information, visit our company website: www.insight-cro.com Email: info@insight-cro.com Telephone: (+2) 233456436 Mobile: (+2) 01093338822 Address: 23 Esraa Al Mohandesin, off Lebanon Street, Giza - Egypt
- الموقع الإلكتروني
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https://www.insight-cro.com/
رابط خارجي لـ Insight - CRO
- المجال المهني
- العيادات الطبية
- حجم الشركة
- ١١- ٥٠ موظف
- المقر الرئيسي
- Mohandiseen, Giza
- النوع
- شركة يملكها عدد قليل من الأشخاص
- تم التأسيس
- 2018
- التخصصات
- Clinical Research، Pharmacovigilance، Vigipx Safety Database، و Literature Search
المواقع الجغرافية
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رئيسي
23 Esraa Al Mohandesin, off Lebanon Street, Giza - Egypt
4
Mohandiseen، Giza، EG
موظفين في Insight - CRO
التحديثات
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أعاد Insight - CRO نشر هذا
📢 Exciting Announcement: Training on the Common Technical Document (CTD) for Regulatory Submissions! 📢 Are you looking to enhance your skills in regulatory submissions? Join us for an in-depth training course on the Common Technical Document (CTD). Who Should Attend: Regulatory Affairs Professionals Quality Assurance Specialists Anyone involved in the preparation and submission of regulatory documents. Course Highlights: In-depth review of the CTD modules according to the latest regulations. Practical guidance on preparing and submitting CTD dossiers. Discussion of the most common deficiencies in the Quality module of the CTD file Hands-on exercises workshop. eCTD overview. CTD for Export (GCC, MENA region, South African, and CIS countries). Course contents and more info: https://lnkd.in/d-jHBu9R Course Details: 🗓️ Date: Local CTD (Registration and Re-Registration new guidelines) : (14/06/2025 & 15/06/2025) CTD for Export: (21/06/2025 & 22/06/2025) 📍 Location: Insight CRO at Mohandesin, Giza. & Online Option Available 💼 Duration: 4 days intensive (2 days for local and 2 days for Export) 🎓 Certificate of completion is provided. Register Now: Visit our registration page: https://lnkd.in/ds_cYGfx Call us: at 01093338822 or send an email to info@insight-cro.com #RegulatoryAffairs #CTDTraining #Pharmaceuticals #Compliance #QualityAssurance
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📢 Exciting Announcement: Training on the Common Technical Document (CTD) for Regulatory Submissions! 📢 Are you looking to enhance your skills in regulatory submissions? Join us for an in-depth training course on the Common Technical Document (CTD). Who Should Attend: Regulatory Affairs Professionals Quality Assurance Specialists Anyone involved in the preparation and submission of regulatory documents. Course Highlights: In-depth review of the CTD modules according to the latest regulations. Practical guidance on preparing and submitting CTD dossiers. Discussion of the most common deficiencies in the Quality module of the CTD file Hands-on exercises workshop. eCTD overview. CTD for Export (GCC, MENA region, South African, and CIS countries). Course contents and more info: https://lnkd.in/d-jHBu9R Course Details: 🗓️ Date: Local CTD (Registration and Re-Registration new guidelines) : (14/06/2025 & 15/06/2025) CTD for Export: (21/06/2025 & 22/06/2025) 📍 Location: Insight CRO at Mohandesin, Giza. & Online Option Available 💼 Duration: 4 days intensive (2 days for local and 2 days for Export) 🎓 Certificate of completion is provided. Register Now: Visit our registration page: https://lnkd.in/ds_cYGfx Call us: at 01093338822 or send an email to info@insight-cro.com #RegulatoryAffairs #CTDTraining #Pharmaceuticals #Compliance #QualityAssurance
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