Medical Drugs Training In USA
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PremiumManufactured by BUCHIbased in SWITZERLAND
Insights into double encapsulation using the Nano Spray Dryer B-90 HP. Explore the possibilities offered by the Nano Spray Dryer B-90 HP to produce particles with sizes less than a ...
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PremiumManufactured by Particle Measuring Systems (PMS)based in USA
On December 20th, 2017, the draft for a Revision of ANNEX 1 (“Manufacture of Sterile Medicinal Products”) of the EU Guideline for GOOD MANUFACTURING PRACTICE for drug products and drug substances was published. This updated guidline will set a milestone for adjustments needed within European agencies overseeing drug products regulatory applications. During the creation process, the ...
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based in USA
Description: This ICH GMP 2-Day seminar will provide your company the opportunity for comprehensive understanding of ICH GMP and the nuances and differences between the three main ICH triumvirate regions (U.S. EU and Japan). It will cover the key areas of how ICH was established, it's goals and objectives, expectations of the healthcare authorities involved and practical differences that you will ...
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based in USA
The bio/pharmaceutical industry is evolving at record pace, accelerated by the challenges of the ongoing global COVID-19 pandemic. Now more than ever, it is important of companies to invest in practical, hands-on training to ensure the continued success of their operations. PDA can deliver the professional training your company needs in the format that works best for you and your employees. ...
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Distributed by EMS1based in USA
As an EMS professional, the focus of care on others may lead you to put your own health on the backburner. To perform your best at work, you must be at optimal health and wellness, especially when traumatic experiences and bodily hazards impact your daily routine. Courses like Bloodborne Pathogens for First Responders, Provider Well-Being, and Responders at Risk: Protecting First Responders From ...
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based in USA
Through our Onsite Training services, ISA can bring our industry-leading instructors, proven training materials, and indispensable hands-on training devices directly to you. You get customized solutions that are highly convenient, cost effective, and flexible-and specially designed to help you improve your productivity and efficiency and avoid unscheduled ...
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based in USA
This medical device software development, verification and validation training package of four courses covers wellIEC 62304 requirements and explains risk based approach for validation using validation protocols and GAMP®. Medical device software can make or break a device. Badly developed, non-compliant software can compromise a device's safety and reliability. These four webinar recording ...
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Manufactured by Mettler - Toledo Int. Incbased in SWITZERLAND
During this free webinar, Donna Blackmond will discuss how the Reaction Progress Kinetic Analysis (RPKA) methodology simplifies kinetic studies of organic reactions. Reaction Progress Kinetic Analysis (RPKA) streamlines kinetic studies by exploiting the extensive data available from accurate in situ monitoring of global reaction progress under “synthetically relevant” conditions, where the ...
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based in USA
The main purpose of stability program is to evaluate a shelf life for a product to enter a market and before that determine a safe stability profile during clinical trial. There are many guidance which showcase the best practices how to achieve a successful stability program and then specific guidelines are formulated for a particular product ex – ICH regulatory guidance, QBD, PQS, ...
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based in USA
The following is a pack of 8 best-selling training CDs for regulatory professionals in the Medical Device industry. These courses provide information on how medical device companies can achieve compliance in the important stages of device development, marketing and ...
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based in USA
This comprehensive training package of 8 courses is aimed at helping medical device companies ensure that their supply chain controls and manufacturing processes comply with existing ...
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based in USA
This Pharma GMP courseware covers all aspects of good manufacturing practices starting from difference between GLP and GMP, vendor selection, supplier agreements & management, raw material risk management, HVAC, GMP environmental control, pharma compressed air, annual product reviews ,deviation investigations, human error reduction ...
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based in USA
DOT Drug and Alcohol Testing per 49 CFR 382 and 40. This online course is designed to meet the DOT regulations and training requirements for Controlled Substances and Alcohol Use and ...
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based in USA
This comprehensive training package of four courses covers clinical trial monitoring techniques, audit procedures and the setting-up of Data Monitoring Committees ...
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Manufactured by Mettler - Toledo Int. Incbased in SWITZERLAND
Increased pressure influences all physical changes and chemical reactions in which a change in volume occurs. For material testing, process development, and quality control there is often no alternative to DSC measurements under pressure. High-pressure DSC allows you to measure samples under defined atmospheres at up to 10 MPa as a function of temperature or time. Higher temperature and pressure ...
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based in USA
This package of 5 training courses is meant to give an exhaustive and in-depth understanding of the Japanese Pharmaceutical Affairs Law (PAL) including the 2005 revisions which are now in ...
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based in USA
This comprehensive training package of ten courses is aimed at helping medical device companies gain a thorough understanding of the top 10 regulations that they should comply ...
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based in USA
This comprehensive FDA inspection training package consists of five training webinar recordings covering everything from preparing for FDA inspections to responding to FDA Form 483s and warning letters. Are you sure you're prepared for an FDA inspection in the new future? Do you think your personnel have received enough training to properly get through an FDA inspection? To help FDA regulated ...
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based in USA
This pack of 4 courses contains some of our best selling Medical Device webinars which together cover the essential compliance challenges faced by Medical Device companies ...
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based in USA
Conducting clinical trials in a rapidly evolving electronic environment presents a unique challenge to the medical device industry where not only quality (GLP/GMP) plays an essential role – but collecting accurate, maintaining viable data (GCP) as part of continuous process improvement (while mitigating risk) is an essential and critical component of the development paradigm. The complexity ...
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