Clinical Trials 2024 | Vancouver | Canada| Clinical Trials Conferences

Clinical Trial Site Management and Business Development

The conduct of clinical trials is one of the most expensive aspects of the development of new medicinal products. It is important, therefore, that the studies should produce high-quality data in the shortest possible time. More companies are trying to use single, larger, complicated trials in an attempt to gain the greatest amount of information about a product and thus reduce the lead time to market. A key element in ensuring this goal is the close cooperation between those responsible for the provision of the clinical trial supplies. The provision of clinical trial supplies is usually organized by a special group, often within the product development department, and it is prudent to discuss a proposed trial with this group at an early stage so that any potential difficulties can be identified and resolved. The major steps in clinical trial supplies are 1)Placing an order for clinical trial supplies, 2) Manufacturing of clinical trial supplies, 3) Blinding of clinical trial supplies, 4) Obtaining comparators, 5) Packaging, 6) Labelling, 7) Documentation, 8) Expiry dating, 9) Dispatch of supplies, 10) Disposal of clinical trial supplies.

The value of some study drugs can reach tens of millions of dollars, making it essential to avoid overproduction, oversupply, and inventory expiration. With the high costs and strict handling requirements for many biopharmaceutical products entering clinical development, the logistics of clinical trial supplies are more critical than ever.

Site management Fundamentals
Site management Innovation
How site selection really works
Management of clinical trial agreements
Accelerating study startup
Financial management of research sites
Marketing & Business development for sites
Improving site compliance

Related Conference of Clinical Trial Site Management and Business Development

November 25-26, 2024

Clinical Trial Site Management and Business Development Conference Speakers

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Regulatory Considerations in Drug Development - Drug Delivery-2024 (France)
Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2025 (France)
Regulatory Updates on Biosimilars - Eurobiosimilars 2025 (France)
Research and development in pharmaceuticals - Drug Safety 2024 (France)
Research and Trials on Oncology and AIDS - Clinical-Trials-2024 (Canada)
Role of Gut Microbiome in Cardiovascular Health - Cardiovascular-2025 (France)
Role of Inflammation in Cardiovascular Diseases - Cardiovascular-2025 (France)
Safety of drugs and pharmacovigilance - Drug Safety 2024 (France)
Smart Drug Delivery Systems - Pharmatech 2025 (Canada)
Smart Polymers for Drug Delivery - Pharmaceutica-2025 (Canada)
Sustainability and Global Health Biotechnology - Biotech-2025 (France)
Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
Targeted Drug Delivery and Controlled Release Systems - PHARMA CONFERENCE-2025 (Czech Republic)
Targeted Therapies - Personalizedmedicine-2024 (Switzerland)
Targeted Therapies in Cardiovascular Regeneration - Cardiovascular-2025 (France)
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Technologies for Formulation - Drug Safety 2024 (France)
Technology in Pharma Sciences - MedTech-2024 (Switzerland)
Telemedicine - Personalizedmedicine-2024 (Switzerland)
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Translational Research - Personalizedmedicine-2024 (Switzerland)
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Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (Czech Republic)
Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (Czech Republic)

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