Medical Drugs Training and Courses

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Webinar: Nanoencapsulation for Drug Delivery

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 ...

By BÜCHI Labortechnik AG based in Postfach, SWITZERLAND. from Webinar Collection Training line

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EU GMP Annex 1 Revision 2017 Draft - Webinar

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 ...

By Particle Measuring Systems based in Boulder, COLORADO (USA).

Good Manufacturing Practices for Pharma Companies - Comprehensive Course ( 8 Modules)

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 ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Pharmaceuticals Training line

21CFR Part 11 and Harmonization with 21 CFR Part 812 for Medical Device Trials

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 in Palo Alto, CALIFORNIA (USA). from Clinical Regulatory Compliance Training Training line

Understanding the JPAL (Japanese Pharmaceutical Affairs Law): Comprehensive Training Package (5 Courses)

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 in Palo Alto, CALIFORNIA (USA). from Pharmaceuticals Training line

Compliant Supply Chain & Manufacturing for Medical Devices - Comprehensive Training Package (8 Courses)

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 ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Medical Devices Training line

EU Medical Device Regulations - Comprehensive Compliance Training Course

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 in Palo Alto, CALIFORNIA (USA). from Medical Devices Training line

FDA Compliant Marketing/Promotions for Pharmaceutical Companies - Best Selling Package Webinar

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 ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Pharmaceuticals Training line

FDA Compliant Marketing/Promotions for Medical Device Companies - Best Selling Package Webinar

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 ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Medical Devices Training line

GMP Training

We provide cGMP training programs to fit for client needs from cGMP orientation new hires through annual cGMP Training on various cGMP Modules. Our new hire cGMP orientation is an overview of basic GMP concepts and emphasizes, to new employees, the importance of understanding and following government ...

By Compliance Global Inc. based in New Hyde Park, NEW YORK (USA).

From Premarket Notification to Recalls - Comprehensive Medical Device Regulations Training Package

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 ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Medical Devices Training line

Top 10 Medical Device Regulations Training (10 Courses)

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 ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA).

Clinical Trials Monitoring - Comprehensive Training Package (4 Courses)

This comprehensive training package of four courses covers clinical trial monitoring techniques, audit procedures and the setting-up of Data Monitoring Committees ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Clinical Research Training line

Product Stability Program - from Drug Development, Clinical Trial and in to Market : Comprehensive Course (4 Modules)

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 ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Pharmaceuticals Training line

Pack of two courses: The essentials of Food and Drug Administration Medical Device Regulations: A primer for manufacturers and suppliers

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 ...

By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Medical Devices Training line