Archive for the ‘Events Calendar’ Category

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

Are you compliant with FDA labeling legislations?

One of the top areas where organizations fall short when audited for FDA compliance is not documenting their standard operating procedures for labeling.

What are you doing to make sure you have the required documentation? (more…)

When serialization could be your answer to global anti-counterfeiting

The supply of counterfeit medicines and medical devices is a growing problem worldwide. The World Health Organization (WHO) estimates that up to 1% of medicines available in the developed world are likely to be counterfeit. This figure rises to 10% globally, although in some developing countries they estimate one third of medicines are counterfeit. (more…)

The Oracle Life Sciences Forum (Geneva)

The fourth Oracle Life Sciences Forum, held in Geneva on the 16-17th March covered a broad range of subjects including clinical development & safety, manufacturing, distribution & operations, customer relationship management and collaboration & architecture.
(more…)

Free Webinar: Reducing the Validation Merry-Go-Round

Any pharmaceutical or medical device manufacturer who does not use validated software, relies on costly manual and paper processes which may compromise the safety, quality and value of its products. (more…)

Labeling Seminar Q&A Session

The following post is a transcript of the Q&A session held recently at the labeling seminar we hosted in Philidelphia on 20th February 2009. It’s a frank discussion between representatives from leading pharmaceutical companies and myself, Product Manager for PRISYM ID. (more…)