Events tagged "Product":

Virtual/Webinar/Webcast

Is your clinical systems production environment bloated with studies that should be archived? Do you long for an easy way to create and refresh a training environment? Are you struggling with the complexities of migrating studies to a new environment? Does your clinical team desire the power of diagnosing production issues in a test environment without having to involve a database administrator? Look no further. Accel-Copy can do all this and more! Read more »

Minneapolis MN, United States

This 3-day class introduces basic principles, techniques, and equipment for the most commonly-used physical and analytical tests on polymeric materials, including: mechanical properties, chemical analysis, combustibility, instrumental analysis, electrical properties, and thermal aging. Read more »

Trifork A/S, Spotorno Alle 4, 2630 Taastrup
Copenhagen, Denmark

There are now several techniques that can help you organize your work, improve your focus and in general help make you more productive. But none of these techniques raise questions about your work brings enough value that will be conducted with sufficient quality is as complete whole way through and actually have an effect in the end. Read more »

Online Event

Why Should You Attend: During the early phases of drug and formulation development, discovery regarding the quality attributes of a new drug substance or a new drug product emerge. Setting specifications is a critical part of the development, as this ultimately defines how a drug product can be considered, safe, effective and of an appropriate quality. Read more »

Online Event

Why Should You Attend:
Most products and technologies contemplated for export from the US fall under the requirements of the EAR. Determining how a product is classified, the controls associated with a classification and eligibility for license exceptions involves a step-by-step process. Read more »

Online Event

Why Should You Attend:
Having a plan for gathering and compiling appropriate sterility assurance documentation to be included in a global marketing application is essential for injectable drug products. In this session we will provide an overview of current regulatory guidance and compendial requirements associated with sterilization validation and control of microbial quality. Read more »

Online Event

Why Should You Attend:
Compliance with compendial standards for residual solvents is required for all drug products provided in the United States, and similar requirements exist in all the major markets of the world. Since every product is unique, and since the requirements refer to over 50 different solvents, achieving compliance can be very challenging. Read more »

Online Event

Why Should You Attend:
Analytical methods play a key role in assuring that drug substances and drug products conform to their specifications. Demonstrating that these methods consistently perform appropriately for their intended purpose can be both challenging and resource intensive. Read more »

Online Event

Why Should You Attend:
Medical products are more complicated and have greater challenges for sterilization process than ever before. These products might include tissue-based products, combination products, devices with drug coatings, devices with batteries or equipped with integrated software, circuits or computer chips. Read more »

Online Event

Why Should You Attend: Medical products are manufactured in environments that are designed to control the level of viable and non-viable particulate and these environments must be monitored to establish that the control measures are continuing to perform acceptably including the impact to product bioburden. Read more »