About

About Sillar Clinical SILLAR CLINICAL provides solutions ranging from the design, over the set-up, to the full management of clinical development projects. Our customers are biotech, medtech, academic institutions and pharmaceutical companies. Our headquarters are located in Ghent, Belgium, at the centre of Europe. To unlock your innovations in medical science and to address your unmet needs at any time, we stay ahead of new regulations in clinical development. We help you thrive via our agile step by step approach. Smart transition from preclinical to clinical. - We simplify the complex of clinical operations for new therapies and technologies. - We think with you by putting pragmatism, creativity and tailor-made solutions at the core of what we do. - We guide you to bring your new medical advances to patients. - We offer a multitalented team to co-create your tasks with the highest level of effectivity and output quality. SERVICES: 1. CLINICAL ARCHITECTURE We think with you and design your clinical development plan. We provide you all the necessary building blocks that suit all your clinical development phases. - Full project management - Clinical development and regulatory strategy - KOL network - Vendor selection and management - Cross-functional expert team - ... 2. CLINICAL OPERATIONS We translate your clinical development plan into practice. We perform operational support to allow for a smart implementation from preclinical to clinical. - Study and protocol design - Study feasibility - Regulatory services - Study start-up - Monitoring services - eTMF management - Data management - Statistics - Study close-out - Medical writing - ... 3. CLINICAL STAFFING Our team of clinical experts is ready to scale your clinical development resources, accelerate timelines, and maximize efficiency throughout your clinical path. - CTM - CRA - CTA - TMF manager - CMC - Regulatory expert - ... SILLAR CLINICAL provides solutions ranging from the design, over the set-up, to the full management of clinical development projects. Our customers are biotech, medtech, academic institutions and pharmaceutical companies. Our headquarters are located in Ghent, Belgium, at the centre of Europe. To unlock your innovations in medical science and to address your unmet needs at any time, we stay ahead of new regulations in clinical development. We help you thrive via our agile step by step approach. Smart transition from preclinical to clinical. - We simplify the complex of clinical operations for new therapies and technologies. - We think with you by putting pragmatism, creativity and tailor-made solutions at the core of what we do. - We guide you to bring your new medical advances to patients. - We offer a multitalented team to co-create your tasks with the highest level of effectivity and output quality. SERVICES: 1. CLINICAL ARCHITECTURE We think with you and design your clinical development plan. We provide you all the necessary building blocks that suit all your clinical development phases. - Full project management - Clinical development and regulatory strategy - KOL network - Vendor selection and management - Cross-functional expert team - ... 2. CLINICAL OPERATIONS We translate your clinical development plan into practice. We perform operational support to allow for a smart implementation from preclinical to clinical. - Study and protocol design - Study feasibility - Regulatory services - Study start-up - Monitoring services - eTMF management - Data management - Statistics - Study close-out - Medical writing - ... 3. CLINICAL STAFFING Our team of clinical experts is ready to scale your clinical development resources, accelerate timelines, and maximize efficiency throughout your clinical path. - CTM - CRA - CTA - TMF manager - CMC - Regulatory expert - ...