Archive for the ‘Life Sciences News’ Category

Jan 23rd

Posted in FDA, Industry News, Knowledge Base, Medical Labeling, PRISYM ClinTrial, PRISYM Medica

The ABC’s of IQ, OQ, and PQ?

LOL, and OMG….today everyone knows what these internet slang terms mean and how to use them.

If you are reading this blog you may also be familiar with Medical Device and Life Sciences specific acronyms for example IQ, OQ, and PQ. For those who are new to the very specific world of Life Sciences, we’ll try to debunk the myths around some of the terminology.

So what is meant by IQ, OQ, and PQ? They are terms that fall under the category of validation and verification.

IQ stands for “Installation Qualification”. The IQ records the installation of the software, and ensures that the installation follows the correct steps.

OQ stands for “Operational Qualification”. The OQ tests or qualifies that the solution is working using test data in general. This maps across to the requirements stated in the Functional Specification, and ensures the product or application meets all the predetermined requirements as stated.

PQ stands for “Performance Qualification” which means that the application, under real life conditions, consistently produces products which meet all predetermined requirements. The PQ is the final test before production (potentially the most important test document you will ever run), testing that the solution works fully in the live environment using live data, and should be based back on a workflow model from your User Requirements Specification.

On top of the IQ/OQ/PQ, you should ensure that you have other key documents including The Validation Master. This will form the detail and coverage of the documentation that you need.

Last thought for the day is that validation requires documented evidence, if the validation process is not documented then it cannot be proven to have occurred. Put another way, your regulatory body will view your validation process as solely a ‘rumour’.

Nov 28th

Posted in Labeling Regulations, Medical Labeling, Technology News

The ‘Falsified Medicines Directive’ and Serialization

The Falsified Medicines Directive published by the Council of the European Union in July is clear legislation aimed at securing the supply chain for pharmaceuticals. But how does this new Directive impact serialization?

First, let’s take at look at the Directive itself. It introduces a number of safety features including:

• Serial numbers and tamper-evident seals for safety packs
• Product traceability through the supply chain
• More stringent rules for the importation of active pharmaceutical ingredients (APIs), plus control and inspections of EU plants manufacturing APIs
• Extended control over the API and medicines supply chain, including improved scrutiny of brokers and traders
• Greater oversight of Internet sales, including an official logo for certified online pharmacies
• More stringent sanctions against counterfeiters

All EU member states have just 18 months to turn the Directive into national law. Manufacturers then have three years be compliant. Although the timetable has been set, there are still some details that need to be finalized. This includes specifics around the unique serial numbers that are required on medicine packs. There is some evidence that it will be the ECC200 2D Datamatrix barcode, but other barcode types and RFID are also being considered.

Whichever method is selected, having an identification and tracking system in place will be the foundation for success for the Directive. This will allow all parties – from manufactures to distributers to pharmacists – to check the authenticity of medication by scanning a unique serial number and checking it against a database. Any duplication of serial numbers or other discrepancies can be immediately flagged and investigated.

As with all previous measures, protecting patients is the fundamental goal of the new Directive. What are your thoughts around the new Directive? Do you think this will be a good way to enforce serialization?

Nov 9th

Posted in Industry News, Labeling Regulations, Medical Labeling

Reintroduction of the Bill HR3026 To Fight Against Counterfeit Drugs

Counterfeit drug revenues were estimated to be in the region of $75 Billion in 2010 and are projected to grow at 13% annually. The World Health Organization stated that it is impossible to quantify the size of the problem but that it may be as much as 10% of the global market.

The scope of the problem in the U.S. is small compared to what other countries like Nigeria and the Ukraine experience, but is the U.S. doing enough to keep out counterfeit drugs? Do you think the current laws we have in place are working?

Just last month U.S. Congressmen re-introduced the bill HR 3026-Safeguarding America’s Pharmaceuticals Act. This bill provides a way for authorities to track, seize and destroy counterfeit drugs before they enter U.S. households. This bill contains several important requirements such as:

• Creating a uniform national pedigree system
• Developing a tracking system, using bar codes and radio frequency tags to enable drugs to be followed
• Authorizing the FDA to destroy seized counterfeit drugs

Are you surprised that a bill like this is NOT already in effect in the U.S? Do you think this bill will pass?

Oct 24th

Posted in GS1, Healthcare Solutions, Life Sciences News, MHRA

Colour-Coded Syringe Labels Increase Patient Safety

The statistics are frightening. With all of the advancements in medical science it’s often oversights and human error that lead to death and serious injury – especially when it comes to medical injections.

• Deaths occur in the UK in approximately one in every 200,000 anesthetics administered. http://news.bbc.co.uk/2/hi/health/medical_notes/4966162.stm
• The preparation of injectable medicines is a highly complex process, involving many steps where errors can happen. Problems in preparing and administering injectable medicines account for 62 per cent of all medication safety incidents reported to the National Reporting and Learning Service (NRLS) as leading to death or severe harm (Safety in Doses, 2009).

In the fast-paced world of surgery and medical treatment, it’s easy for a mistake to be made and the wrong medication or dosage to be administered to a patient. To help alleviate this problem, a joint initiative by the Royal College of Anaesthetists, the Association of Anaesthetists of Great Britain and Ireland, the Intercollegiate Faculty of Accident and Emergency Medicine and the Intensive Care Society recommends using a single standard for syringe labelling. The recommendation includes adopting a colour-coded labelling system that is currently used in North America and APAC.

PRISYM ID and Codonics make it easier for hospitals and healthcare providers to adopt these standards, as well as other barcode and labelling criteria, with a safe labelling system for syringes called the Codonics Safe Label System (SLS) 500i. The SLS 500i (designed and manufactured in the USA) was developed by Massachusetts General Hospital anaesthesiologists to prevent intravenous medication errors via barcode assisted medication labelling. The technology scans drug vial barcodes, and prints a full-colour label containing labelling data elements recommended by the initiative. Click here for more information on SLS 500i.

Any steps that can be taken to reduce human error and anaesthetist’s reliance on memory when it comes to administering injectable drugs will be a step forward. We expect the healthcare industry will continue to focus on labelling standardisation, the use of protocols and checklists, and the elimination of look-alike products as a way to help ensure patient safety. What have you observed regarding labelling protocol? Has the new colour-coding system had an impact on safety? Share your thoughts and predictions.

Aug 25th

Posted in FDA, GS1, Life Sciences News, PRISYM Medica

FDA UDI Regulations – An Updated Look at the Timeline

In June 2010 PRISYM ID hosted a webinar titled, “Tips for Implementing FDA UDI without Derailing Production”. Featured speakers included Jay Crowley from the FDA and Janice Kite from the GS1 Global Office. The webinar gave an overview of UDI (Unique Device Identification) in practical terms and went through the planned timeline for proposed FDA UDI regulations.

Now that a year has passed, we thought it would be beneficial to provide you with an updated timeline around FDA UDI. While nothing is official, the following is the most recent information on how the FDA UDI rollout might look:

12 Months after the FDA UDI Standard is Published (2013)

The first set of deadlines focus on Class III Medical Devices. These are devices that support or sustain human life, are of substantial importance in preventing impairment of human health, or present a potential unreasonable risk of illness or injury to the patient, such as implantable pacemakers, replacement heart valves, automated external defibrillators, and implants.

• UDI will apply to all levels of packaging
• An engraved UDI may be required for some Class III medical devices
• If a device has a serial number, the UDI will also be serialized

36 Months after the FDA UDI Standard is Published (2015)

The next class of medical devices to be effected is Class II, which are items like x-ray systems, gas analyzers, pumps, and surgical drapes.

• UDI will apply to all levels of packaging

60 Months after the FDA UDI Standard is Published (2017)

The final group is Class I Medical Devices, such as tongue depressors, arm slings, examination gloves, and hand-held surgical instruments.

• UDI will probably just apply to the device (not packaging)

Medical devices are classified by intended use and potential risk to the patient, and as you can see from the timeline above, the UDI regulations address the most critical devices first. The years listed are based on the FDA UDI standard being published in 2012, which is the current plan. Stay tuned!

Aug 16th

Posted in Events Calendar, FDA, Industry News, Knowledge Base, Labeling Regulations, Life Sciences News, Medical Labeling, PRISYM Medica, Technology News

IQPC Pharmaceutical Serialization and Traceability 2011 – Geneva

We are looking forward to attending IQPC’s Pharmaceutical Serialization and Traceability conference coming to Geneva in November. The conference will focus on topics that are very important to us, such as patient safety and anti-counterfeiting.
One of the featured speakers for the event, Janice Kite, Director Healthcare Traceability for GS1, participated in our “Tips for Implementing FDA UDI without Derailing Production” webinar. At the Geneva event, Janice’s presentation, “Traceability and Product Serialization Standards and Harmonization”, will cover key worldwide regulatory and industry developments, GS1 Standards for Healthcare, how GS1 standards assist in compliance to the Directive for Falsified Medicines and the standardization strategy across Europe and Internationally.
The conference will also have industry speakers from the EFPIA, APB and PGEU, GIRP and HIBC as well as from manufacturers AstraZeneca, Roche, Boehringer-Ingelheim, GlaxoSmithKline, Daiichi-Sankyo and Abbott Laboratories.
If you are planning to attend this event, be sure to use ‘19085.002Prisym’ to get a 20% discount on the standard conference prices. You can register in one of three ways:

Go online: http://www.pharmaserialisation.com/Prisym
Call: +44 (0)207 368 9300
Email: enquire@iqpc.co.uk

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