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- Data integrity, regulatory compliance solutions for pipette user training sector
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Undefined Training Courses Near Namibia
6,271 training items found
by:ComplianceOnlineĀ Ā 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 experts and ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
Computer system validation and risk-based verification and validation planning to meet US FDA and ISO 13485 ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
This pack of two training courses provides 2 hours of training on analysis of the sections of the QSR design control ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (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 ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (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 ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
This medical device software development, verification and validation training package of four courses covers wellIEC 62304 requirements and explains risk based approach for validation using validation protocols and GAMP®. Medical device software can make or break a device. Badly developed, non-compliant software can compromise a device's safety and reliability. These four webinar recording ...
by:ComplianceOnlineĀ Ā 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 ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
Clinical Labs are a tough environment to be in. Not only are there a multitude of rules, there are a number of areas which are not very clearly defined. On top of all this, the rules keep changing all the ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
The following training is a pack of 10 best-selling training CDs for the microbiology lab. These courses provide solutions for all critical challenges faced by microbiology lab professionals pertaining to regulations/compliance, best practices, quality, ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
The following training is a pack of 10 best-selling training CDs for the Laboratory. These courses provide solutions for all critical challenges faced by Laboratory professionals pertaining to regulations/compliance, best practices, quality, etc. ComplianceOnline has created these trainings individually through world renowned experts and combined together to create a comprehensive course for ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
This JAPAN Regulatory compliance training is designed to provide an overview of the regulatory environment in Japan with respect to regulatory filings and registrations. With the 2005 revisions to the Japanese Pharmaceutical Affairs Law (PAL), foreign life science companies are eyeing on the opportunities created in Japanese market for them. It becomes imperative to understand the overall ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
This comprehensive training package of three courses is aimed at helping clinical laboratories ensure compliance with CLIA ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
This comprehensive training package of four courses covers clinical trial monitoring techniques, audit procedures and the setting-up of Data Monitoring Committees ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
Learn the nuances of food safety and labelling requirements such as Sanitary Control of Product and Services, application of NOM-051-SCFI/SSA1-2010, basic requirements of the Canadian Food label, requirements for the location and size of the common name, net quantity declaration, list of ingredients and allergen labeling, identity and principal place of business, date markings, nutritional ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
This food preservation and packaging comprehensive training package of five courses is aimed at food manufacturers and covers US and EU regulations related to alternative food preservation techniques and food contact ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
This comprehensive training package of five courses covers the control of foreign material and pathogens in food manufacturing as well as food recall handling ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
The following training is a pack of most informative and top selling training CDs on topics related food safety compliance in 2012. These courses provide details on how to implement the best practices for food safety for your unit/organization/product pertaining to regulations/compliance, best practices etc. ComplianceOnline has created these trainings individually through world renowned experts ...
by:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
Many regulated companies have not brought their old products up to current FDA standards and are not in total compliance. This webinar defines the criteria to be used for medical products design history file remediation. For example companies should be compliant to 14971:2007. Design History Files need to be updated to meet current standards. The FDA expects risk management to be integrated into ...
by:ComplianceOnlineĀ Ā 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:ComplianceOnlineĀ Ā based inSan Jose, CALIFORNIA (USA)
Many organizations are still struggling to understand their processes, to identify the cost of quality and to make necessary process improvement through an effective decision making and team work in order to stay competitive in today’s global economy. In order to achieve this goal while at the same create a data-driven organization, all of the basic and advanced quality tools are there to ...

