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April 2017 Blog Posts (17)

4 eco-friendly safety essentials to help save the world

The health and safety sector and the green sector now thankfully meet with a selection of products that are effective in preventing harm to workers, while also benefitting the environment. Such developments are important factors in the modern workplace, which wants to keep employees safe and now also wants to reduce its carbon footprint and do its bit for the…

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Added by Alex on April 28, 2017 at 7:00am — No Comments

The art of writing effective audit observations

Audits are a means of evaluating operations and other functions of an organization. ISO 19011:2011 Guidelines for Auditing Management Systems describes audits as a process used for gathering the evidence of verifiable documents and map their suitability, alignment and fulfilment with the company’s policies and procedures.

An audit is an important tool that helps organizations to analyze opportunities, implement best practices, and assess all the important factors in…

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Added by Adam Fleming on April 27, 2017 at 6:29am — No Comments

Article on “A Tour of the FDA”

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Added by John Robinson on April 27, 2017 at 5:50am — No Comments

Good Manufacturing Practices are essential for ensuring quality

Key Takeaway:

GMPs are critical for the manufacture and distribution of foods, drugs and other pharmaceutical products. These need to be implemented diligently by organizations that are involved in these products.

Quality is a great concern for a manufacturer and consumer of any product. To ensure that quality is maintained across a variety of products ranging from foods to pharmaceutical products; a few guidelines are required. These guidelines…

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Added by John Robinson on April 26, 2017 at 8:06am — No Comments

Article on “Statistical Sampling Plans for Medical Devices”

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Added by John Robinson on April 21, 2017 at 6:04am — No Comments

Understanding the ways of conducting shrink investigations

Shrink investigation is essentially about examining the causes of shrink (loss) in retail businesses. Although retail is one of the fastest growing areas of business, the possibility of shrink is very high in this area. It is also an overlooked area, because of which many shrinks that could otherwise have been prevented, do not get prevented.

Controlling losses is as important…

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Added by Adam Fleming on April 21, 2017 at 6:02am — No Comments

Leadership Management Academy 201-202: Rising Through the Management Ranks 2017

Overview:

Why Should You Attend?

By attending, you will take advantage of a great opportunity to advance as a manager to the next level!

Too often, we focus on getting things done and results and miss working on our self-development. Let’s face it: this is how we get paid yet this is also how we keep…

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Added by John Robinson on April 20, 2017 at 7:20am — No Comments

Writing error-free procedures while complying with GMP regulations

In the area of GMP regulations, procedures are very vital, for both execution and audits. It is always true that the greater the clarity and comprehensiveness with which these procedures are written; the easier it becomes for users to use them without missing important information for regulators.

Despite the advent of technology into almost all the areas of GMP regulations; there is still the existence of the human factor. It is still the major…

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Added by Adam Fleming on April 19, 2017 at 6:43am — No Comments

Rising in one’s career through leadership management

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Added by John Robinson on April 19, 2017 at 5:09am — No Comments

Packaging and labeling are important components of commercial and clinical products

Packaging and labeling of commercial and clinical products are very important aspects to an organization involved in a business that relates to these products. While the packaging and labeling of commercial products is important, it is more so with clinical products, because these products play an important role in a clinical trial and also in the very life of a patient or subject.

Commercial products have their own value over time. The FDA has guidances for…

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Added by Adam Fleming on April 17, 2017 at 8:41am — No Comments

FDA and EU requirements on data integrity and implementation

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Added by John Robinson on April 17, 2017 at 5:49am — No Comments

Are Your Test Methods Ready for Quality Control or any laboratory ?

The FDA considers verification and transfer of Test Methods a subject worthy of 483 observations and issuance of Warning Letters. Test method verification is also required by the GMPs, and USP has a whole chapter dedicated to test method verification. This makes comprehension of the requirements for the verification and transfer of a test method into a laboratory imperative for Laboratory Managers and other personnel.…

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Added by Adam Fleming on April 12, 2017 at 6:42am — No Comments

Applied Statistics for FDA Process Validation 2017

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Added by John Robinson on April 12, 2017 at 5:29am — No Comments

How the supposed microbial control or monitoring approach SHOULD be handled.

That water systems are critical to the pharmaceutical industry is a given. This fact makes it absolutely imperative for pharmaceutical companies to get a grasp of the techniques needed for getting these systems right. Product recall, costly downtime and many other related negatives are some of the consequences of not getting these matters right.

Among the primary causes,…

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Added by Adam Fleming on April 10, 2017 at 6:24am — No Comments

Procurement and Contract Fraud is usually off -the books- and difficult to detect and investigate

In this interconnected, interdependent global world, the need for contracting procurement of any goods or services is strong and indispensable. However, the benefits of this feature notwithstanding, there are several loopholes in the procurement and contracting activity. Outsourcing and contracting, by their very nature, are vulnerable to fraud. Fraud can happen at any stage of the procurement and contract process.…

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Added by Adam Fleming on April 6, 2017 at 5:59am — No Comments

What to expect during GMP Inspection

Regulatory agencies such as the FDA conduct inspections for product-related Good Manufacturing Practice (GMP) in the course of assessing an application for marketing approval. The basic purpose of product-related GMP inspections is to check for compliance with the GMP guidelines set out in the International Conference on Harmonization (ICH) and national and local GMP regulations. GMP is the slightest standard that a manufacturer has to mandatorily meet in its production…

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Added by Adam Fleming on April 3, 2017 at 6:29am — No Comments

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swethakumar posted a blog post

Where to study the NEBOSH Course in Bangalore?

NEBOSH is a UK-based board conveying professional qualifications based on Occupational Health and Safety Management which has the syllabus to evaluate the workplace health and safety issue with proper preventive measures.NEBOSH Training in Bangalore by Green World Group is accredited by the international HSE awarding bodies like IOSH, IEMA, and IIRSM.This qualification has been designed for all kinds of people such as individuals, Managers, Supervisors, and Employees who require more extensive…See More
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Shaun Alex posted a blog post

The 5 Best Outlets for Promotional Products in New York, New York

The most densely populated and the most populous city of the nation, New York is rightly labeled as the global power city of the USA. Not only does it serve as a dominant node for the global economic network, but in fact, it has been described as the cultural, financial and media capital of the world as well. The city also serves as the residing home of the United Nations’ headquarters. The impact which it imbues can be felt across various channels and mediums of supremacy for arts, commerce,…See More
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Training Doyens posted an event
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Harassment, Bullying, Gossip, Confrontational and Disruptive Behavior: A Manager’s Guide on How to Detox and Neutralize a Negative Workplace at Training Doyens 26468 E Walker Dr, Aurora, Colorado 80016

November 19, 2019 from 1pm to 2:30pm
OVERVIEWBad attitudes, jealousy and disruptive behavior will sabotage hospital morale, lower self-esteem and reduce teamwork and productivity. When toxic behavior infects a department, managers may be tempted to ignore it or give in, the wrong thing to do, but tolerating it is not a solution!This session will show you how to neutralize gossip and put a system in place to…See More
9 hours ago

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EdbMails Office 365 Backup Software

Security approaches are principal to any organization’s protection and survival strategies. There are advanced types of attack that happen each day to take classified organization reports. To protect…Continue

Started by johnjorge 13 hours ago.

How to export EDB to PST successfully?

Microsoft Exchange Server maintains the data in EDB file format such as priv1.edb where it stores the private data of user mailbox, pub1.edb stores public data of user mailbox, .stm where these files…Continue

Started by marina paul on Friday.

Reasons for Office 365 email backup

The security enhancements and ease of access from anywhere are some of the major reasons why many organisations are willing to make the switch to the cloud from on-premises Exchange Servers.While…Continue

Started by johnjorge on Friday.

How EdbMails successful in deleted mailbox items recovery?

Are you wondering on how to get back your deleted mailbox items? Don’t be tensed to do the recovery of deleted mailbox items just go with EdbMails EDB to PST Converter tool that will show you how you…Continue

Started by clara dsouza on Thursday.

How EdbMails Exchange recovery reliable than manual methods?

When I immersed on manual method I couldn’t get actual result? Is there any other way to get successful result?Yes, Exchange server recovery third party tool works better, but how? Refer this…Continue

Started by marina paul on Wednesday.

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