Drug Analysis Training For Medical Monitoring
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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
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
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
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 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 CANADA
The need to prevent impaired persons from affecting safety in the workplace cannot be overstated. Recent changes in Occupational Health and Safety (OH&S) Legislation, together with better informed employers, has brought forth a realization that serious attention must be given to ensuring that employees arriving to the workplace are ...
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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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based in USA
This pack of 2 courses contains the essentials of FDA Medical Device regulations. In the United States, the US Food and Drug Administrates Medical Devices through several different regulations, the principle one is the Quality System Regulation 21 CFR 820 (QSR). Other regulations include Registration and Listing, Labeling, Medical Device Reporting, and Corrections and Removals (Recalls). This ...
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based in CANADA
This online Alcohol & Drug Testing: Driver Awareness course provides drivers with information about the Department of Transportation’s (DOT) alcohol & drug testing requirements as they relate to 49 CFR ...
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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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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
As per 49 CFR Parts 40, 199.241 (for pipeline operators)and 382.603 (for motor carriers) this online course for Drug & Alcohol Reasonable Suspicion Training for Supervisors is designed to meet DOT regulations and training requirements for Controlled Substances and Alcohol Use and Testing. The Department of Transportation requires any supervisor who sends or refers employees for drug and/or ...
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based in INDIA
What is Computer Aided Drug Designing Training Course ? We at RASA life science informatics in Pune , India conduct Computer Aided Drug Designing Training Course or CADD Training Course in accordance to the recent trends in the industry. Our Insilico Drug Disigning training Course contains detailed knowledge about the different methods and techniques taught in a more practical manner. If You Want ...
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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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based in USA
This comprehensive training package of 7 courses is aimed at helping companies to be compliant and streamline the robust supply chain planning, processes, risk management etc by maintaining regulatory guidelines. Implementing Robust Supply chains for life-sciences companies are important now and growing in importance as device manufacturers outsource products and services low cost destinations it ...
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