Clinical Trials Training For Pre-Clinical
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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 four courses covers clinical trial monitoring techniques, audit procedures and the setting-up of Data Monitoring Committees ...
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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
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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by Marcus Evansbased in UNITED KINGDOM
This section is built to advance professional skills in the pharmaceutical sector. Courses are designed to meet the specific needs of Product and Project managers and those responsible for CRM, Brand and Marketing within the pharmaceutical industry. All courses are intensive, case study and discussion driven, and led by experienced trainers with many years practical experience in the ...
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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
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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Manufactured by Summus Medical Laserbased in USA
Start your therapeutic laser journey with live interactive and hands on training where you will learn about using the laser including: Navigation System, Treatment Guidance, Clinical Applications, Safety Protocols, Patient Education, Treatment Protocols & ...
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based in USA
The following is a pack of 4 best-selling training CDs for sales, marketing & regulatory professionals in the Pharmaceutical industry. These courses provide solutions for all critical challenges & questions faced by you and your team pertaining to regulations/compliance, best practices, etc. ComplianceOnline has created these courses individually through world renowned experts and ...
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Manufactured by NovaDigm Therapeutics, Inc.based in USA
Staphylococcus aureus (S. aureus) is the leading cause of skin and soft tissue infections (SSTI), also referred to as skin and skin structure infections. Methicillin-resistant S. aureus (MRSA) is a predominant cause of hospital- and community-acquired SSTI. Recent studies conducted by the US Department of Defense Tricare health system have estimated rates of S. aureus SSTIs (54% MRSA) among their ...
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based in USA
Medical devices cannot be shipped to Europe unless they are in full compliance with the European Medical Device Directive (MDD). The compliance requirements vary, depending on the classification of the device. It's not just the CE marking requirements that manufacturers and exporters have to worry about, but also the way the MDD is linked to the EU Clinical Trial Directive and ISO Certification ...
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based in USA
The following is a pack of 3 best-selling training CDs for regulatory professionals in the Medical Device industry. These courses provide information on how medical device companies can achieve compliance with the EU Medical Device Directive, obtain CE marking and fulfill ISO ...
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based in USA
The following is a pack of 4 best-selling training CDs for sales, marketing & regulatory professionals in the Medical Device industry. These courses provide solutions for all critical challenges & questions faced by you and your team pertaining to regulations/compliance, best practices, etc. ComplianceOnline has created these courses individually through world renowned experts and ...
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