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Safety Training Info

New Training requirement and what is OSHA citing companies on

Website: http://hpsafetyconsulting.com
Location: Houston
Members: 7
Latest Activity: Dec 26, 2015

Discussion Forum

Safety Trainer Needed

Dear Colleagues, Nationally we are looking for qualified, independent instructors who would be willing to work part time teaching safety courses that are specifically tailored to meet the identified…Continue

Started by Frank Subzda Feb 18, 2013.

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Latest Activity

Adam Fleaming posted a blog post

Is important to involve managers in project management audits

Project management is one of the core areas of expertise in today’s corporate career. Defined as a temporary allocation of resources to accomplish a defined goal and objective; project management may be considered the building blocks of an organization’s business. Given the importance of project management to any business; it is imperative that the organization implements a set of checks and balances into the whole system of project auditing to ensure that its project management is on track to…See More
yesterday
Roger Steven posted a blog post

Implementation of Regulatory Aspects of Clinical Research is critical

Implementation of Regulatory Aspects of Clinical Research is criticalOne of the prime areas of clinical studies is regulatory aspects of clinical research. This applies in almost equal measure to medical research as a whole. The FDA and other regulatory bodies have…See More
yesterday
Chris Trottier posted a blog post

Injury Free? Safety is not just a number

Safety is a goal. Safety is a mentality. Safety is effort.  Safety is a work in progress.  Safety is something every company should treasure. A quick look around and you’ll see professionals, organizations, schools and businesses touting their unwavering dedication to safety. But what does that mean?  Some will point to their low incident…See More
Wednesday
Adam Fleaming posted a blog post

What are the Steps involved to Create a Bullet Proof 510(K)

A medical device has to mandatorily make a submission for premarket approval (PMA) to the FDA to demonstrate that the device to be marketed is substantially equivalent or at least as safe and effective as a non PMA-subjected legally marketed device. This submission is called 510 (K).A medical device company has to submit a product for PMA when it manufactures or makes changes and modifications that could substantially affect safety and effectiveness requirements under 21 CFR 807 and design…See More
Wednesday

Discussion Forum

Safety Trainer Needed

Dear Colleagues, Nationally we are looking for qualified, independent instructors who would be willing to work part time teaching safety courses that are specifically tailored to meet the identified…Continue

Started by Frank Subzda Feb 18, 2013.

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