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Showing posts with label iCertify. Show all posts
Showing posts with label iCertify. Show all posts

Monday, December 6, 2010

The FDA Enters Education E-Style


The FDA, in its process improvement program, is enhancing education for companies and consumers on the FDA website, www.FDA.gov.
CDRH is the first center to add course material at CDRH Learn, www.fda.gov/Training/CDRHLearn.  Most material is available in three languages: English, Spanish and Chinese.  Courses offered are in most medical device regulations, regulated software, BIMO and the 510K process.  The e-learning posted represents the areas that lead in lack of compliance for medical device folks with the code of federal regulations.  Most educational courses that are currently listed are focused on the health care industry, manufacturers and clinicians.

For those of use seeking to enhance our knowledge on regulations, it represents a good starting point.  However, it will not stop the foolish manufacturers who continue to rack up 483s, Warning Letters and other noncompliance notifications by willful violation.  It may assist the unwitting violator, who broke the regulations because they were unclear or unlearned.  The courses do not replace annual site training in the good manufacturing practices.

Can we guess why FDA has done this? We shouldn't have to.  Over the last two decades, many companies have reduced their budgets for employee education.  This has become evident by the fall-off in professional conference attendance.  Companies don't have the time to train employees in groups on site, and conference costs continue to rise. A company may send one employee to a conference and expect them to return to the site and train others. - a common practice that often falls short in follow-through and substance.  Trying to bring a conference on-site also becomes expensive.

QPharma offers both Lunch & Learns and customized onsite training, as well as compliant e-Learning for the entire organization.  Lunch & Learns consist of one hour programs on hot button FDA topics; never a sales pitch and as the name states, lunch is on us.  Customized training solutions are offered on a fee basis.  They represent truly site specific training.  They are more detailed, transparent to the client’s own education platforms and tailored for the client site’s processes.  They represent better value as the instructor is not lecturing to a mixed audience, but a group with specific needs; and since CDRH is the only FDA center offering e-learning, QPharma can supply your needs from specifics on the other centers, such as CDER, CVM and CBER. We take education seriously, considering the environment we come from!

Monday, May 24, 2010

Breaking News! FDA to Audit Pharma's Electronic Recordkeeping

We sent our valued clients and colleagues this update last week, but for those of you who are not on our mailing list...

The FDA will begin auditing pharmaceutical companies electronic recordkeeping capabilities to evaluate the industry’s compliance with 21 CFR Part 11.



According the article by Ed Silverman of Pharmalot, “…the FDA is about to begin a series of so-called inspectional findings at many drugmakers… The precise timing and number of facilities to be audited - and these are audits, in effect - has yet to be determined, but they will be conducted by the FDA’s Center for Drug Evaluation and Research, or CDER.”


To view QPharma’s webinar on how to stay Part 11 compliant with your training systems, visit our website here. Simply register on the site to take advantage of the Part 11 recording that, when aired live, attracted over 200 attendees from 7 different countries worldwide. It also contains a high-level overview of iCertify 3.0, QPharma's 21 CFR Part 11 Compliant training system for the life science industry.

For the full article, click here: PharmaLot