Pharmaceutical Production Training For Medical Drugs
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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 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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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
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 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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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 Water system compliance training will give you a comprehensive knowledge about water system compliance with relation to Microbial Quality Problems, Microbial Testing, Endotoxin control, Sanitization, Water system validation. Water can be a major source of microbial contamination in the manufacturing systems for Medical Devices, Diagnostics, Pharmaceuticals, and Biologics fields, as well as ...
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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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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 TSK Groupbased in CANADA
TSK aesthetic training partners offer aesthetic courses for all experience levels. TSK Laboratory offers you a unique opportunity to attend a highly-specialised medical aesthetic masterclasses led by multi-award-winning tutors and key opinion leaders. In these aesthetic training courses, elite tutors will share their in-depth knowledge and experience through one to one guidance and detailed ...
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based in USA
This presentation will review a methodology for implementing Risk-Based Validation of test equipment, facilities and analytical instruments used in GLP, cGMP and GCP facilities. A case study is presented for the construction qualification, relocation and new equipment installation for a cGMP facility. The cost and time savings associated with using risk-based validation will be presented. Over ...
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based in 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 ...
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based in 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, ...
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based in 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 ...
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based in 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 ...
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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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Manufactured by Mettler - Toledo Int. Incbased in SWITZERLAND
Development of continuous processes is a chemical engineering challenge that requires a balance of heat transfer, mass transfer and kinetics. This webinar discusses how to simulate plant conditions and develop continuous ...
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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 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 ...
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