Saturday, January 30, 2010

Multivitamins Seem Benign, Maybe Beneficial

Fruit on display at La Boqueria market in Barc...Image via Wikipedia
We might never really know for sure in my lifetime. I take them because I think my diet isn't diverse enough.

In any event, here's an interesting read published by the Washington Post, Evidence is thin that multivitamins are beneficial, but they seem benign

Learn more about vitamins:
- in this FDA video, Fortify Your Knowledge About Vitamins (video)
- read this book, The Complete Idiot's Guide to Vitamins and Minerals, 3rd Edition

Do you take them? ... and why?

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Wednesday, January 27, 2010

FDA CDRH Announces 2010 Strategic Initiatives


There's a lot here. I recommend you view this or download the FDA PDF, CDRH FY 2010 Strategic Priorities.

Here's what you'll find:

Executive Summary
Priority 1. Fully Implement a Total Product Life Cycle Approach
Strategy 1.1. Enhance and Integrate Premarket, Postmarket, and Compliance Information and Functions
Strategy 1.2. Improve Guidance and Regulation Development
Strategy 1.3. Develop a Cross-Center Compliance Strategy
Priority 2. Enhance Communication and Transparency
Strategy 2.1. Develop a Strategic Approach to Public Communication
Strategy 2.2. Improve Internal Communications
Strategy 2.3. Increase Transparency in Decision Making
Priority 3. Strengthen Our Workforce and Workplace
Strategy 3.1. Recruit, Develop, and Retain High-Quality Employees
Strategy 3.2. Leverage External Expertise
Strategy 3.3. Establish Pathways for Resolving Differences of Opinion
Strategy 3.4. Improve Internal Administrative Processes
Strategy 3.5. Make CDRH's White Oak Facilities More Workplace-Friendly
Priority 4. Proactively Facilitate Innovation and Address Unmet Public Health Needs
Strategy 4.1. Foster Development of Medical Devices to Respond to Unmet Public Health Needs
Strategy 4.2. Develop a Personalized Medicine Program

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Monday, January 25, 2010

Pharmaceutical Manufacturing Handbook - Regulations and Quality - free online book

Checkout this free online book by Shayne Cox Gad:

Pharmaceutical Manufacturing Handbook - Regulations and Quality
Here's what's inside the book:
  • Section 1:  Good manufacturing practices (GMP)
  • Section 2:  International regulation of good manufacturing practices
  • Section 3:  Quality
  • Section 4:  Process analytical technology (PAT)
  • Section 5:  Personnel
  • Section 6:  Contamination and contamination control
  • Section 7:  Drug stability
  • Section 8:  Validation
Buy this book:  


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Saturday, January 23, 2010

FDA Says Watch Out For Fake Alli Capsules

The U.S. Food and Drug Administration (FDA) is warning consumers about a counterfeit and potentially harmful version of Alli 60 mg capsules (120 count refill kit).  The counterfeit Alli product looks similar to the authentic product, with a few notable differences. The counterfeit Alli has:

  • Outer cardboard packaging missing a “Lot” code;
  • Expiration date that includes the month, day, and year (e.g., 06162010); authentic Alli expiration date includes only the month and year (e.g.,: 05/12);
  • Packaging in a plastic bottle that has a slightly taller and wider cap with coarser ribbing than the genuine product;
  • Plain foil inner safety seal under the plastic cap without any printed words; the authentic product seal is printed with “SEALED for YOUR PROTECTION”;
  • Contains larger capsules with a white powder, instead of small white pellets.

Consumers who believe they have received counterfeit Alli are asked to contact the FDA's Office of Criminal Investigations (OCI) by calling 800-551-3989 or by visiting the OCI Web site (http://www.fda.gov/OCI).




Related Posts:
Counterfeits In The Global Drug Supply

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Wednesday, January 20, 2010

Counterfeits In The Global Drug Supply


More bad news about fake drugs getting into the global drug supply.  This Chemical and Engineering News article is very well written, Fake Pharmaceuticals - Those fighting against counterfeit medicines face increasingly sophisticated adversaries.

Here are my takeaways:
  • "The best “guesstimate” is that 1% of drugs in the developed world are counterfeit. In developing nations, between 10 and 50% of drugs are thought to be fake."
  • "Is it possible to stop medicines counterfeiting altogether? I doubt very much whether it is. All we can do is to try our best to secure the supply chain."
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Related Reading: Making a Killing: The Deadly Implications of the Counterfeit Drug Trade

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Monday, January 18, 2010

2010 - Border inspections and delays for device and import - more FDA presence

metamorphicImage via Wikipedia
Devicemakers and importers can expect delays for inspections and screenings because the FDA is putting their trainees at US borders, reports FDAnews Device Daily Bulletin, Devicemakers May Face More Inspections, Delays in 2010:
"New employees probably will be trained at the borders because that’s where the highest volume of regulated commodities can be found"
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Saturday, January 16, 2010

Electronic Cigarettes - Update - Ruling Stops FDA From Blocking Importation


A federal judge says the FDA (Food and Drug Administration) overstepped its authority in efforts to regulate electronic cigarettes, reports this Washington Post article, FDA can't block importing of 'electronic cigarettes'.

The FDA's position:
FDA says they've found cancer-causing ingredients in the products, despite manufacturers’ claims that they are safer than tobacco cigarettes.

The judge's position:
Electronic cigarettes are “the functional equivalent of traditional cigarettes."

Bottomline:
U.S. District Judge Richard J. Leon determined that electronic cigarettes are tobacco products and are not subject to restrictions.

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Monday, January 11, 2010

More Pharma 2010 Trends

... and even more pharma trend predictions for 2010.

Tracy Staton reports in What's the outsourcing outlook for 2010?, what we can expect in 2010 from an outsourcing perspective.

In summmary, expect:

  • Outsourcing won't let up in 2010
  • Outsourcing to heat-up in sales, IT, and CROs 
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Wednesday, January 6, 2010

Avoid The DOJ - FCPA Violations - Foreign Corrupt Practices Act

Seal of the United States Department of Justic...Image via Wikipedia
I never heard about the FCPA (Foreign Corrupt Practices Act) until reading about it today. Wikipedia says FCPA addresses accounting transparency requirements under the Securities Exchange Act of 1934 and another concerning bribery of foreign officials.

Anyways, FDANews reports that the Department of Justice’s (DOJ) FCPA and healthcare fraud units are beginning to work together to investigate FCPA violations in the device and pharmaceutical industries. The DOJ has more information about FCPA on their website.

Here's why you need to care. The DOJ wants to aggressively enforce and investigate violations of the FCPA, targeting pharmaceutical and medical device companies as well as their individual executives and board members; this leaves them open to potentially massive legal and financial liabilities.

Additional Resources:
Bribery Abroad: Lessons from the Foreign Corrupt Practices Act

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Monday, January 4, 2010

FDA Reports Another Extortion Scam by FDA Impersonators


The FDA is warning the public about criminals posing as FDA special agents and other law enforcement personnel as part of an international extortion scam.

It goes something like this. The criminals call the victims (who in most cases previously purchased drugs over the Internet or via "telepharmacies") and identify themselves as FDA special agents or other law enforcement officials. The criminals inform the victims that purchasing drugs over the Internet or the telephone is illegal, and that law enforcement action will be pursued unless a fine or fee ranging from $100 to $250,000 is paid. Victims often also have fraudulent transactions placed against their credit cards.  The criminals always request the money be sent by wire transfer to a designated location, usually a foreign county. If victims refuse to send money, they are often threatened with a search of their property, arrest, deportation, physical harm, and or incarceration.

Anyone receiving a telephone call from a person purporting to be an FDA or other law enforcement official who is seeking money to settle a law enforcement action for the illegal purchase of drugs over the Internet should refuse the demand and call the FDA’s Office of Criminal Investigations Metro Washington Field Office at (800) 521-5783 to report the crime.

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Saturday, January 2, 2010

Lots Of Hangover Cures To Try

New York Times Square New year celebrations in...Image via Wikipedia
Whether you're trying to recover from the New Year celebration or not, check out these suggested cures.

I ran across this list of 17 hangover cures on Epicurious, Hangover Cures 17 helpful foods for the big-head blues.  I found it pretty entertaining, and decided I wanted to see something a little more serious.

So checkout this MSN Video, Holiday Hangover Cures, it walks through how to prevent a hangover, what to do while you're drinking, and last but not least, what to do if you get a hangover.

Cheers!

Previous Posts:
Booze Good For You in 6 Ways

For Wine Lovers:
Wine Lovers Dishwasher Magnet

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Booze Good For You in 6 Ways

Tempranillo varietal wine bottle and glass, sh...Image via Wikipedia

This MSNBC News article, Cheers! 6 ways a little booze does the body good, gives six good reasons to rationalize your drinking habit.

In summary:
  1. Women who drink occasionally may live longer.
  2. Moderate drinking may actually protect your brain — especially if you’re a woman.
  3. Women who drink moderately are less likely to develop high blood pressure.
  4. A few drinks a week might keep the heart doctor away.
  5. White wine may help you breathe better.
  6. Drinkers exercise more than teetotalers — and the more people drink, the more they exercise.
I'm not endorsing drinking, and thought you'd be interested in this collection of reported health benefits.

Previous Posts:
Say No To Drugs PSAs - Public Svc Announcements over the yrs
Series About Wine And Your Heart
Dementia - Mod Drinking Good - Heavy Drinking Bad
Up To Moderate Drinking And Socializing Good For You

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Champagne In The Freezer - Reminder Magnet

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From SkillsPlus International Inc.

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Even More Resources, Books, & Things (many from Amazon.com)

FDA, GMPs, QSR, GCP, GLP, GXP:
21 CFR Parts 210 and 211: Drug Industry GMP's     Compact Regs Parts 807, 812, and 814: CFR 21 Parts 807, 812, and 814 Medical Device Approval (10 Pack)     The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices     Compact Regs Part 11: CFR 21 Part 11 Electronic Records; Electronic Signatures (10 Pack)     How to Fail an Fda Quality Audit: A Look at Some of the Causes of Failure to Comply With Fda Quality Regulations     Pharmaceutical Master Validation Plan: The Ultimate Guide to FDA, GMP, and GLP Compliance     How to Develop and Manage Qualification Protocols for FDA Compliance         Agent GXP FDA Part 11 Guidebook: The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, For Pharmaceutical, Medical Device, Food, ... Trials and GCP (Good Clinical Practices)     Development of Fda-Regulated Medical Products: Prescription Drugs, Biologics, and Medical Devices     FDA Regulatory Affairs: A Guide for Prescription Drugs, Medical Devices, and Biologics     Design and Analysis of Clinical Trials: Concepts and Methodologies (Wiley Series in Probability and Statistics)     Clinical Studies Management: A Practical Guide to Success     Analytical Chemistry in a GMP Environment: A Practical Guide     Process Validation in Manufacturing of Biopharmaceuticals: Guidelines, Current Practices, and Industrial Case Studies (Biotechnology and Bioprocessing Series)     Pharmaceutical Equipment Validation: The Ultimate Qualification Guidebook     Preclinical Drug Development (Drugs and the Pharmaceutical Sciences)     Group Sequential Methods: Applications to Clinical Trials (Chapman & Hall/Crc Interdisciplinary Statistics Series)     Validation Standard Operating Procedures: A Step by Step Guide for Achieving Compliance in the Pharmaceutical, Medical Device, and Biotech Industries, Second Edition     Pharmaceutical Stress Testing: Predicting Drug Degradation (Drugs and the Pharmaceutical Sciences)     Cleaning Validation: A Practical Approach     Validated Cleaning Technologies for Pharmaceutical Manufacturing     Risk-Based Compliance Handbook     Microbiology in Pharmaceutical Manufacturing, Second Edition, Revised and Expanded, Volume I (1)     Microbiology in Pharmaceutical Manufacturing, Second Edition, Revised and Expanded (Volume 2)     Bioprocess Validation: The Present and Future     Laboratory Validation: A Practitioner's Guide     Quality Assurance Workbook for Pharmaceutical Manufacturers     Risk-based Software Validation: Ten Easy Steps     ISO 13485 and FDA QSR Internal Audit Checklist     ISO 13485:2003 & FDA QSR (21 CFR 820) Quality Manual, 34 Procedures and Forms
Training Resources:
1001 Ways to Reward Employees     Planning Programs for Adult Learners: A Practical Guide for Educators, Trainers, and Staff Developers, 2nd Edition     50 Creative Training Openers and Energizers     Personalized M&M Candies     Oriental Trading Co - Training toys and supplies     GMP Training Gifts & Giveaways     GMP Training & Quality Posters