Navigation Links
PharmaChk Device for Substandard, Counterfeit Drug Detection Receives Saving Lives at Birth Transition-to-Scale Grant
Date:8/7/2014

Rockville, MD (PRWEB) August 07, 2014

With the potential to revolutionize how medicines regulators, customs agents, procurement agencies, warehouse personnel, health facilities, and other providers throughout the world detect poor-quality medicines, a new portable device called PharmaChk will be supported with a $2 million transition-to-scale grant from Saving Lives at Birth: A Grand Challenge for Development. The funding will help further PharmaChk’s development and bring it closer to commercial production and availability.

“The toll that poor-quality medicines take on global public health—particularly among the most vulnerable populations in the developing world—is staggering, with 99% of all maternal deaths occurring in developing countries,” said Ronald T. Piervincenzi, Ph.D., chief executive officer of the U.S. Pharmacopeial Convention (USP). “Helping to ensure patient access to good quality drugs—including those for used for neonatal care, to fight infectious diseases or to maintain good maternal health—is a leading priority for USP.”

Portable and easy-to-use, PharmaChk is being developed in conjunction with researchers at Boston University (BU) to detect and quantify active ingredients in medicines. The ability to screen for potential medicines quality problems can be a tremendous benefit to healthcare personnel treating patients and to regulators and health program officials responsible for tracking and ensuring the quality of their medicines. This holds especially true in Sub-Saharan Africa and in Asia where national borders are often porous and tracking the flow of medicines from country to country can be extremely challenging.

According to Patrick Lukulay, Ph.D., USP’s vice president of global health impact programs and director of the Promoting the Quality of Medicines (PQM) program funded by the U.S. Agency for International Development (USAID), “Having the appropriate amount of an active pharmaceutical ingredient is key for any medicine to be effective. A poor-quality medicine can be one without enough active ingredient, which can lead to both preventable disease progression and to the development of drug resistance in patients and the community. In other cases, a medicine may have the correct amount of active ingredient but be of poor quality—for example not dissolve properly or contain impurities—due to poor manufacturing or storage practices, which can also compromise the medicine’s ability to bring a clinical benefit to the patient.”

PharmaChk—which was named as one of Scientific American magazine’s “World Changing Ideas of 2013”—has been in development by scientists from Boston University (BU), with support from the PQM program and seed funding from the Saving Lives at Birth partnership. Building country capacity to address public health concerns posed by counterfeit and substandard-quality medicines has been a long-standing goal of PQM, a 10-year program managed by the USAID Office of Health Systems of the Bureau for Global Health, with the aim of strengthening country health systems and improving health outcomes. A scientific organization dedicated to creating quality standards for medicines, food ingredients and dietary supplements, USP works collaboratively with USAID to implement PQM.

Launched in 2011, the Saving Lives at Birth partnership includes USAID, the Government of Norway, the Bill & Melinda Gates Foundation, Grand Challenges Canada (funded by the Government of Canada), and the U.K’s Department for International Development. Saving Lives at Birth is a global call for groundbreaking, scalable solutions to prevent infant and maternal deaths around the time of birth and supports a wide variety of work across maternal and neonatal health, family planning, nutrition and HIV.

While other methods to screen for substandard or counterfeit products in the field are currently available, they are limited in their ability to quickly and accurately quantify the actual amount of active ingredient in a sample as well as to determine how quickly that active ingredient dissolves so it can work in the body as intended.

This past spring, the first pilot study using PharmaChk on medicine samples was conducted at USP’s Center for Pharmaceutical Advancement and Training (CePAT) in Accra, Ghana. USP opened CePAT in May 2013 to help expand the number of trained experts and available tools to combat substandard and counterfeit medicines that threaten nations in Sub-Saharan Africa.

The pilot study was conducted of samples of the antimalarial medicine artesunate, collected from three main medicine sources in Accra—public hospital/clinics, private retail/wholesale pharmacies, and informal outlets. USP and BU scientists are excited about early results from the pilot study, and plans are underway to further refine PharmaChk and to use the device to test samples of other medicines collected from the field.

Read the full story at http://www.prweb.com/releases/2014/08/prweb12080802.htm.


'/>"/>
Source: PRWeb
Copyright©2014 Vocus, Inc.
All rights reserved

Related medicine news :

1. Daily Sun Exposure and Vitamin D Intake Simplified With Wearable Device
2. Exercise Device Helps With Squats - Designed by InventHelp Client (LGI-1774)
3. New hand-held device uses lasers, sound waves for deeper melanoma imaging
4. Laparoscopy Devices Market: Internal Closure Devices, Energy Systems, Trocars, Laparoscopes, Irrigation Systems, Insufflation Devices, Sample Retrieval Bags
5. J&J's Ethicon Unit Recalls its Power Morcellator Devices After Warnings by Federal Regulators and Concern About Risk of Spreading Occult Cancer, Parker Waichman Comments
6. Turkey Pharmaceutical and Medical Device Market Worth $21.5B & $3.3B by 2020 Respectively, Says a Report Available at MarketOptimizer.org
7. New Dental Device Reviews to Stop Snoring by VitalSleep
8. Have You Had a Hysterectomy or Removal of Uterine Fibroids? Morcellator Device Withdrawn From Market Due To Cancer Risk
9. Orthopedic Trauma Fixation Devices Market: Global Forecast, Share, Size, Growth and Industry Analysis 2014 - 2020
10. Loffler Companies Introduces New Konica Minolta bizhub PRESS C1085/C1100 and Canon imagePRESS C800/C700 Devices
11. NiQ Health Reveals the Extensive Use of Unregulated Medical Devices in Australian Hospitals
Post Your Comments:
*Name:
*Comment:
*Email:
(Date:1/17/2017)... ... January 17, 2017 , ... A prescription medication bottle, pocket knife, luggage ... Cradle to Cradle Product Design Challenge , the Cradle to Cradle Products Innovation ... circular design challenges scheduled to run through early 2018. The challenges are presented by ...
(Date:1/17/2017)... ... 2017 , ... SC&H Group, a leading audit, tax, and consulting firm, announced ... Advisory Services practice . Rossi is the third technology consulting leader to join SC&H ... grows, and the practice continues to expand.     , Bringing more than 25 years of ...
(Date:1/17/2017)... ... January 17, 2017 , ... The Sharie Withers ... has announced the latest beneficiary of their thriving community involvement program. The current ... to fulfilling the dreams of terminally ill patients. Donations to this worthy cause ...
(Date:1/17/2017)... Falls, NJ (PRWEB) , ... January 17, 2017 ... ... and Learning Center and the Montclair State University’s Athletic Training Education program forged ... State University’s Athletic Training Education Program, which is consists of both student ...
(Date:1/16/2017)... York, NY (PRWEB) , ... January 16, 2017 , ... ... grand opening of a new showroom in East Hanover, New Jersey. , “We are ... Gym Source. “The new innovative in-store concept is designed to give clients a seamless ...
Breaking Medicine News(10 mins):
(Date:1/17/2017)... -- Research and Markets has announced the addition of ... to their offering. ... The global fluoropolymer market in the healthcare industry to grow ... Global Fluoropolymer Market in the Healthcare Industry 2016-2020, has been ... experts. The report covers the market landscape and its growth prospects ...
(Date:1/17/2017)... , Jan. 17, 2017 Following an ... today praised the Food and Drug Administration,s (FDA,s) ... Human Drug Products by Pharmacies and Outsourcing Facilities." ... proposed limitation on pre-packaging -- which would have ... costs to long term care (LTC) pharmacies.  ...
(Date:1/17/2017)... ReportsnReports.com adds "Anaphylaxis - Pipeline Review, H2 2016" ... Anaphylaxis,s therapeutic pipeline with comprehensive information on the therapeutic development ... assessment by drug target, mechanism of action (MoA), route of ... featured news and press releases. ... Complete report on H2 2016 pipeline ...
Breaking Medicine Technology: