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Jul 30, 2015

My eQMS Consultant is Gone—Now What? 4 Post Go-Live Survival Tips


As users begin to learn the software, they will 
have lots of questions. Will you be ready?  
by Stephanie Jones, Senior Professional Services Consultant, MasterControl

In my April 9, 2015 post, I offered eight tips for planning a seamless software go-live. This post picks up where that one left off to answer an important question many clients wrestle with after a successful go-live: What do you do when your software implementation consultant is no longer part of your day to day operations?

Having participated in hundreds of software implementations, as both a user and a consultant, I have found that so much focus is placed on getting through the actual go-live process that customers often forget there’s one final implementation hurdle to clear: incorporating the application into their daily business activities.

If you’ve recently completed a successful software go-live, congratulations! You probably think you can relax and go back to your real job. Sorry—but that’s just wishful thinking.

Jul 28, 2015

Three Keys to Successful FDA Inspections – Preparation, Management and Follow Up


Atlantic Validation

Successfully completing a FDA inspection is critical to cGMP operations and commercial success.  Implementing and maintaining robust quality systems is one element to accomplishing this goal.  However, it is not the only element.  Inspection preparation and management is another, equally important element to ensure a successful outcome.  In fact, proper Inspection management techniques can help mitigate the risk of receiving an observation for compliance gaps.  This article will provide insight on understanding the inspector, discuss how to prepare for and manage the actual Inspection, describe follow-up activities required for close-out, as well as describe real-life lessons learned.

Jul 23, 2015

Quality Event Investigations, Interviews, and Brian Williams


LearningPlus

If you are a follower of television news, you undoubtedly know of the problems that Brian Williams, the NBC television network news anchor experienced in early 2015.  (If you hadn’t heard, he was found to have embellished his experience as a passenger as he was flying in a military helicopter in Iraq while covering a news story.  He claimed his helicopter was hit by antiaircraft fire, when, in actuality, it was the lead helicopter; his aircraft was not affected [1].)  In April 2015, it was reported that there were other exaggerations attributed to him [2].

There are two different views we can take in considering how Mr. William’s story changed over time.  On one hand, his exaggerations might be blamed on showmanship or intentionally telling the proverbial “fish that got away” story. On the other hand, his inflation of the facts could be due to what happens when one’s memories are saved, retrieved, subtly changed, resaved, and then found to have drifted considerably from the original event [3]. (Either case is a bad situation for a journalist to put himself in.)   If we think of it this way, Mr. William’s predicament provides a learning opportunity for those involved in deviation and quality event investigations.

Jul 21, 2015

European Supply Chain: A Series of New Regulations in Force



Director Operations
CONCEPT HEIDELBERG GmbH

The new EU Directive 2011/62/EU and its delegated acts keep on changing the pharmaceutical supply chain. The directive introduced numerous Delegated Acts with different time schedules and had some impact on revisions of several chapters of the EU-GMP Guidelines.

Here is the status quo of the Directive and the delegated acts:

Already in 2011, the European Commission published Directive 2011/62/EC, the so-called Falsified Medicines Directive (or FMD).The main goal was the fight against counterfeit medicines. In 2014 the technical characteristics of one key requirement were defined, the unique identifier delivering the possibility of verification of the authenticity of single folding boxes. This will be a 2D barcode (data matrix). As this new requirement will become active in 2018, it is time to start defining strategies for both technical implementation and change control strategy.

Jul 16, 2015

Get Products to Market Sooner by Systematizing Quality Cycles



Getting a product to market is not a one-time event—it involves a series of cyclical processes. Is every phase along your organization’s ongoing quality continuum as efficient as it should be?


by James Jardine

Marketing Communications, MasterControl


Creating a product and getting it to market is not a one-time achievement. It entails a series of ongoing cyclical processes.

It all starts with an initial idea developed with a collaborative team. Input is gathered from all the necessary sources and then tweaks to the original concept are made as needed. Many different types of reviews, approvals, and regulatory checks are also required during this development stage. Then it’s time to provide suppliers or vendors with specific orders to ensure all the puzzle pieces will fit together as planned. Once your organization’s employees receive all the training they need to make the product according to the specifications that have been devised it feels like you’ve almost reached the finish line. Now you just flip a switch and watch as the magic is made while you celebrate your magnificent accomplishment, right?

Jul 15, 2015

eMDR Compliance Deadline Looms: Last Minute Tips for Procrastinators


 Beginning August 14, 2015, device makers must 
submit all medical device reports electronically.

by Alex Butler, Product Manager
Life Science Applications (LS APPs), MasterControl   

In February of 2014, the FDA issued a final rule amending 21 C.F.R. Part 803, Medical Device Reporting, to require medical device manufacturers and importers to submit initial and supplemental MDRs in an electronic format via the Electronic Submissions Gateway (ESG), rather than in paper form through Form FDA 3500A. The compliance deadline of August 14, 2015, is fast approaching! Will you be ready?

Here are some last minute tips for going all electronic.

Jul 14, 2015

Don't Just Fix It: Find It Before Your Customer Does

When mistakes happen in your 
company,  who takes the blame?
by Anna Thornton
Analytics Operations Engineering


It is human nature to find a single cause of a problem, fix it, and assume everything is fine. In fact, the use of a scapegoat is documented in writings from four thousand years ago. All of the sins of a community were laid on the head of a single goat that was then driven into the wilderness, relieving every one of their problems. Four millennium later, we still believe in the power of the scapegoat to take away problems. When a product fails in the hands of a customer, triggering a recall or creating excessive warranty costs, companies quickly find a solution (or fire someone) and assume all is well. Mistakes are embarrassing and it is easier to assume they won’t happen again. The GM recall case is a classic example of this. News articles focus on one or two issues: the engineer who signed off on the change or the automotive safety reporting requirements. Everyone is pointing a finger at each other.

Jul 9, 2015

Ensuring Proper Training for Clinical Research Staff in Less Time



President & CEO, IMARC Research


There has never been a more exciting time to be involved in clinical research. We’re seeing more advances in life-changing medical devices and pharmaceuticals than at any other time in history, creating a growing demand for qualified clinical research associates.

The U.S. Bureau of Labor Statistics estimates jobs for medical scientists will grow by 13 percent [1] from 2012 – 2022.

It only makes sense then that clinical research professionals need continuing education to keep up with a rapidly evolving industry.

Jul 8, 2015

It’s Hot in Here—Quality, Compliance, and Romance

Editor, MasterControl Insider

Sun, spice, and romance—they’re everything I associate with summer. And I’m not talking about your love life, but your quality system.

Indulge me for a moment and let me talk about the two things—quality software and romance—that preoccupy me most. I’m a full-time marketing writer and a newly published romance author. By day, I write about quality and compliance. By night, I write about people who live happily ever after (known as HEA to romance readers).

It’s no wonder that two of my colleagues asked me (read: it sounded very much like a dare) to link romance with quality management system. It took me about 60 seconds to realize that, in fact, establishing a QMS or overhauling an existing system is similar to finding and nurturing a romantic relationship.

Jul 7, 2015

From Open Payments to OpenFDA, the Push for Global Transparency is Accelerating

Transparency leads to happier patients, 
better trials and lower costs, advocates say.
 

by Lisa Weeks, Marketing Communications Specialist, MasterControl


Transparency has been a hot topic in life science circles in recent years. So hot, in fact, that it has almost become a buzzword, which implies that it lacks real substance or staying power. Transparency advocates, who are pushing to make health industry data—everything from clinical trial results to procedure pricing information—more accessible, would disagree.