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Updated by akash kumar on Apr 30, 2014
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akash kumar akash kumar
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complianzworld

Complianz World is established to impart high quality training on governance, regulations and compliance (GRC) through webinars and seminars. We are passionate about processes, procedures, safety and regulations across industries. We value an individual’s right to obtain high quality services and products without discrimination or difference. We understand the importance of compliance to established standards, practices and regulatory frameworks

Exporting to Canada Procedures and Documentation

Participants of our live events, may cancel up to 48 working hours prior to the event start date and will receive a letter of credit to be used towards a future event, valid up to one year from the date of issuance. We at "Complianz World" would process/provide refund only if the event has been cancelled.

For More Details Click Here.

FDA regulations, FDA compliance Training

Get Online Trainings, webinars and seminars on FDA regulations standards and best practices from renowned experts. Complianz World, a leading GRC training provider, brings a range of topics related to FDA regulations that apply to all industries in the life science space - Good manufacturing practices (GMP), Good clinical practices (GCP), Good laboratory practices (GLP), FDA enforcement actions, Warning Letters, Quality and safety standards, CAPA, Data management and documentation, Verification and validation, Packaging and labeling etc.

Purchasing Card Compliance with IRS Guidelines

Participants of our live events, may cancel up to 48 working hours prior to the event start date and will receive a letter of credit to be used towards a future event, valid up to one year from the date of issuance. We at "Complianz World" would process/provide refund only if the event has been cancelled.

Good Practices for Q-Submission and 510(k) Submission

This [webinar] will provide an opportunity to get familiar with an FDA’s pre-submission process (Q-submission or Q-Sub) to effectively communicate with the FDA early in the regulatory process in an effort to better prepare for a sustainable 510(k) submission and clearance.

For More Details Click [Here].