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Pharmaceutical Training Courses In Usa
26 training items found
by:NetZealous LLC based inFremont, CALIFORNIA (USA)
With our wide ranging experience of having been in the Continuing Professional Education (CPE) arena, we at NetZealous are well placed to offer immaculately designed training courses for the pharmaceutical industry. This is another of the areas in which we have our ears to the ground. We understand the workings of this industry and are well-versed with all the regulations and ...
by:Trinity Consultants based inDallas, TEXAS (USA)
This one-day course provides background and guidance on EPA’s National Emission Standards for Pharmaceuticals Production (“Pharmaceuticals MACT”). Course content will include background information on the MACT program, analysis of applicability criteria, and a summary of the standards, monitoring, recordkeeping, and reporting requirements. ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
Water can be a major source of microbial contamination in the manufacturing systems for Medical Devices, Diagnostics, Pharmaceuticals, and Biologics fields, as well as consumer products and cosmetics companies. There are many standards proposed by different associations and industry bodies related to different aspects of water system compliance. Some of these are quite dated and ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (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, ...
by:Parenteral Drug Association (PDA) based inBethesda, MARYLAND (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. ...
by:Parenteral Drug Association (PDA) based inBethesda, MARYLAND (USA)
An Environment Dedicated to Learning. PDA offers a variety of training courses at its Training and Research Institute (TRI) facility, located at PDA's Global Headquarters in Bethesda, ...
by:The International Society of Automation (ISA) based inResearch Triangle Park, NORTH CAROLINA (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 ...
by:NSF International Strategic Registrations, Ltd. based inAnn Arbor, MICHIGAN (USA)
NSF International's on-site training provides cost savings, personalized attention and the ability to customize the curricula. Employees appreciate the ability to spend less time away from home and the office as well as the opportunity to proactively solve problems with the focus and spotlight on their unique ...
Manufactured by:Mettler - Toledo Int. Inc based inGreifensee, 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 ...
by:COBBLESTONE, a Division of The Center for Professional Advancement (CfPA) based inEast Brunswick, NEW JERSEY (USA)
For products that claim a desired Sterility Assurance Level (SAL), proof of a defined SAL (specification) is achieved through the product’s sterilization and sterility assurance controls. Compliance Observations cited each year by the FDA on Form 483s that relates to Sterilization and Sterility Assurance processes shows that there are deficiencies associated with these key processes that ...
by:COBBLESTONE, a Division of The Center for Professional Advancement (CfPA) based inEast Brunswick, NEW JERSEY (USA)
In the FDA’s Guide to Sterilization Process Controls, the FDA stated five (5) key inspectional objectives which are used by the agency during routine inspections of sterilization and sterility assurance processes. One of the key areas of concern pertains to the production and process control subsystem (including sterilization process controls) which requires that manufacturers of products ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
ComplianceOnline has created these courses individually through world renowned experts and combined them together to create a comprehensive training resource for companies to train their employees. You can store it as a library material and train all your employees in these compliance issues to get them ready to face any kind of compliance challenge and overcome it through expert advice and best ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
This Medical Device Software Development & Management package training will have 4 courses which covers FDA's Medical Device Software Regulation, Medical Device Software Verification and Validation, IQ / OQ / PQ Approach and IEC ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
The following is a pack of 5 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 maintenance. In today's complex regulatory environment, medical device manufacturers often find that the road to compliance can be ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
This comprehensive training package is aimed at helping medical device companies ensure that their supply chain controls and manufacturing processes comply with existing regulations. This comprehensive training package is aimed at helping medical device companies ensure that their As manufacturing becomes increasingly global, with responsibility for various parts of the final product vesting with ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (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 ...