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When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.
Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.
In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.
Learn moreRemember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.
Before any new drug product is launched, it must first be shown through clinical studies that it is safe and effective. The cornerstone of these studies is the clinical supplies. Unless these supplies are prepared and labeled correctly, patient safety could be compromised and expensive clinical trials may be in jeopardy.
The aim of this 90-minute accredited online training is to provide a high-level overview and introduction to the key aspects involved in designing a clinical supply chain which is fit for today’s rapidly evolving trial landscape. Emphasis will be placed on the optimal design for labels, packaging and global supply logistics.
This training is important to the industry since examples will be provided of strategies that can be employed to ensure the overall supply chain can work flexibly with changes in clinical trial design.
The introductory training will provide an overview of the key procedures and techniques involved in the preparation of clinical trial supplies. The training is intended for those who are new to clinical supplies or individuals who may interact with clinical supplies personnel/third party providers and want to understand the clinical supply chain or re-fresh their knowledge.
• Pharmaceutical
• Biotechnology
• Contract Clinical Research (CRO)
• Contract Clinical Packaging and Logistics
This online training will benefit professionals in the following industries:
• Packaging
• Clinical Manufacturing
• Clinical Trial Label Design
• Clinical Research Associate
• Logistics
• Quality Assurance/Quality Control
• Interactive Voice Response Systems- IVR/IWRS
In addition, this training will benefit, hospital pharmacists involved in Clinical Trials in departments such as:
• Quality
• Research and Development
• Clinical Supplies
• Clinical
Danielle DeLucy, MS
Owner, ASA Training & Quality Consulting LLC
Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 23 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations. Danielle began her QA career as a Quality Control Pharmaceutical Microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the Quality management arena while increasing her responsibility. She has helped to lead many Regulatory Health Inspections and was instrumental in the coaching process of her peers prior to any inspection. Currently, Danielle assists companies who are faced with warning letters, consent decrees and those wishing to improve compliance establish more robust quality systems so that the company can succeed.