Clinical Trials 2024 | Vancouver | Canada| Clinical Trials Conferences

Clinical Trial Supply Management

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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.

Clinical Trial Supplies Market by Products & Services (Logistics & Distribution, Manufacturing, Packaging and Labeling), Phases (Phase I, Phase II, Phase III) & Therapeutic Areas (CNS & Mental Disorders, Cardiovascular, Oncology) - Global Forecast to 2020. The clinical trial supplies market is expected to reach USD 1,274.3 million by 2020 from USD 904.3 million in 2015, at a CAGR of 7.1%. The global clinical trial supplies market is segmented based on products and services, phases, therapeutic areas, and regions. The logistics and distribution services segment is expected to register the highest growth rate in the clinical trial supplies market, by products and services, during the forecast period. The high growth in this segment is attributed to the globalization of clinical trials and increasing outsourcing services.

The major factors contributing to the growth of the clinical trial supplies market include globalization of clinical trial activities, increasing R&D investments and government support, and rising incidences of various diseases. Furthermore, increasing expansion activities by CROs is another major factor driving the growth of this market.

Building an action plan in CTS
Site management in clinical research
Selection and benefits of CTMS
Fundamentals of outsourcing in clinical devices
Globalization & Outsourcing
Strategic or tactical outsourcing

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Radiation-based medicines and biotherapy - Drug Safety 2024 (France)
Rational Design of Non-Oral Drugs - PHARMA MEDICINAL CHEMISTRY 2025 (Canada)
Rational Drug Design and Molecular Modeling - PHARMA CONFERENCE-2025 (Czech Republic)
Real-World Evidence in Clinical Trials - Pharma Europe 2025 (Italy)
Recent Advancements in Medicinal Pharma - PHARMA MEDICINAL CHEMISTRY 2025 (Canada)
Reformulation Research - Drug Safety 2024 (France)
Regenerative Medicine and Tissue Engineering - Drug Delivery-2024 (France)
Regulatory Affairs and Drug Safety - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
Regulatory Affairs and Intellectual Property Rights - Future Pharma 2025 (Netherlands)
Regulatory Affairs and Quality Assurance in Pharmaceutics - Pharmaceutica-2025 (Canada)
Regulatory Authority Compliance - MedTech-2024 (Switzerland)
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)
Targeting the Renin-Angiotensin-Aldosterone System (RAAS) - Cardiovascular-2025 (France)
Technologies for Formulation - Drug Safety 2024 (France)
Technology in Pharma Sciences - MedTech-2024 (Switzerland)
Telemedicine - Personalizedmedicine-2024 (Switzerland)
The BBB for drug delivery - Drug Safety 2024 (France)
The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
The Next Generation Approach of Antibiotics - Antibiotics Resistance 2024 (Canada)
Therapeutic Drug Transporters - Drug Safety 2024 (France)
Translational Research - Personalizedmedicine-2024 (Switzerland)
Translational Research in Pharmacology and Therapeutics - NURSING PHARMACOLOGY 2024 (Netherlands)
USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
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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