September 25-29, 2017 Hyatt Regency McCormick Place, Chicago, IL
New Look, New City, Same Remarkable Event on Temperature Controlled Life Science Supply Chain
As the global healthcare industry grows, temperature controlled logistics rapidly evolves along with it. With ever-changing global regulatory requirements, a more diverse array of biopharma products entering the supply, and new technology emerging daily; companies face the challenge of constantly adapting their supply chain processes to stay ahead of the curve.
Responding to the evolution within the industry, the 15th Annual Global Forum has changed as well with an updated look, color scheme, and topic focus. This elevated brand identity allows us to follow suit with the industry, remain at the forefront of innovation, and embody the high level of quality the event delivers each year.
Introduction November 27th is the US deadline for serializing packages and cases! Will you be ready?
Along our journey with our business partners in achieving SERIALIZATION, a number of questions keep popping up relative to the different Manufacturer and Wholesaler requirements. To help answer these questions we have created the following timeline that includes:
1) a summary of the requirements,
2) reference to the applicable regulatory acts and guidance.
Please share comments, and let us know we can help with any of your Serialization or compliance needs.
We look forward to celebrating your SERIALIZATION success in 5 months!! Sequence Serialization team
Adents and Sequence Team up for New Serialization Webinar
In this webinar, 5 Key Points for a Future Proof Drug Serialization Solution, Sequence is pleased to team up with Adents to highlight the complexity of preparing for the impending DSCSA regulations, specifically pharmaceutical serialization. Matt Brawner, Sequence Director, Sales Execution and Jim Cummings, Adents VP, Partners will lead this discussion on June 23, 2017 at 11:00 AM EST.
Collectively, we will provide answers to the 5 key questions on everyone’s mind when assessing a serialization solution such as:
How to Adapt to Long Term Compliance with Evolving Regulations
How to Orchestrate Multiple Hardware and Devices
How to Ensure a Quick and Effective Roll-Out
How to Maintain your OEE
How to Optimize your Qualification Process
Drug serialization is becoming a major challenge for the pharmaceutical industry as regulations will soon be in place in more than 40 countries. The deadline for compliance with the DSCSA is rapidly approaching. Whether you are a pharma company, a contract manufacturer or contract packager, you will need to have a serialization and track & trace solution up running by November 2017
The good news is that the road to serialization now has a passing lane: a full-featured, future-proof, compliance ready-serialization solution combining a premium-performance software, a large choice of hardware and access to a global network of certified solution partners enabling to easily and quickly address current and future regulatory requirements.
Adents is a Premier Serialization Solution Company with more than 25 years of experience in unique product identification and traceability. Adents helps pharma companies and CMOs comply with regulatory requirements quickly and turn serialization data into Business Intelligence
Adents Seriza is the first standardized Line-Level and Site-Level serialization solution that is fully configurable, remarkably flexible and highly scalable. Seriza provides pharma companies with everything they need to protect their brand, fight against counterfeits, control their supply chain, analyze customer behavior and enrich their marketing data. All this, while maintaining overall equipment efficiency (OEE) and minimizing drops in productivity.
Cold Chain GDP & Temperature Management Logistics Global Forum- IQPC Pharma Logistics Week
MAY 22-25, 2017 | HOTEL DEL CORONADO, CORONADO, CA
Throughout the pharma supply chain, there have been new regulations, players, and demands that are taking place and need to be addressed. Within the pharmaceutical world, patient care has become more imperative than ever as has the cohesive relationship between the numerous departments in the supply chain!
Sequence, Inc. provides scalable and customizable monitoring solutions for temperature, humidity, CO2, pressure, particle counting and open/close relays for your specific needs. Whether you have a cold chain drug product, controlled incubators containing your critical stability samples, low temperature freezers containing valuable cell banks or biologics, refrigerators used for day-to-day laboratory operations, or warehouse space requiring continuous monitoring, our Sequence Monitoring Center is capable of providing personalized around the clock support to ensure product/materials are maintained under your specified conditions. The Sequence Monitoring Center currently supports clients across all 50 states and is experienced in the installation, configuration, calibration, validation, quality oversight, and continuous monitoring support of your product, equipment, and/or facility. Through our client dedicated support module, our 24 hour call center, and our ability to provide vendor management, quality oversight and remediation, we are able to provide our clients a complete solution for monitoring support and compliance no matter where the client is located across the globe.
The BIO International Convention is hosted by the Biotechnology Innovation Organization (BIO). BIO represents more than 1,100 biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other nations. BIO members are involved in the research and development of innovative healthcare, agricultural, industrial and environmental biotechnology products.
BIO performs many services for members, but none of them are more visible than the BIO International Convention. The BIO International Convention helps BIO fulfill its mission to help grow the global biotech industry. Profits from the BIO International Convention are returned to the biotechnology industry by supporting BIO programs and initiatives. BIO works throughout the year to create a policy environment that enables the industry to continue to fulfill its vision of bettering the world through biotechnology innovation.
The key benefits of attending the BIO International Convention are access to global biotech and pharma leaders via BIO One-on-One Partnering, exposure to industry though-leaders with over 1,500 education sessions at your fingertips, and unparalleled networking opportunities with 16,000+ attendees from 76 countries.
Bio-IT World Conference & Expo was once again a great success. The 2016 meeting brought together more than 3,300 attendees from 41 countries to navigate the new era of precision medicine and build collaboration across the industry.
With over 13 tracks, 14 pre-conference workshops, and three industry awards, the 2017 Bio-IT World Conference & Expo promises to be bigger than ever with more expert content, more industry insights, and more opportunities to build relationships that will drive the bio-IT industry forward.
We just need one thing: Your voice is crucial to the conversation. Please join us in Boston, May 23-25, as we work together to advance bioinformatics and life sciences.
About Bio-IT World Conference & Expo
Since its debut in 2002, the Annual Bio-IT World Conference & Expo has established itself as a premier event showcasing the myriad of IT and informatics applications and enabling technologies that drive biomedical research, drug discovery & development, and clinical and healthcare initiatives. The Bio-IT World Conference & Expo continues to be a vibrant event that unites 3,300+ life sciences, pharmaceutical, clinical, healthcare, and IT professionals from more than 40 countries.
Spanning three days, the 2017 meeting includes 13 parallel conference tracks and 14 pre-conference workshops. Compelling talks, including best practice case studies and joint partner presentations, will feature over 260 of your fellow industry and academic colleagues discussing themes of big data, smart data, cloud computing, trends in IT infrastructure, omics technologies, high-performance computing, data analytics, open source and precision medicine, from the research realm to the clinical arena.
Access All 13 Tracks for One Price
Network with 3,300+ Life Sciences, Pharmaceutical, Clinical, Healthcare and IT Professionals
Hear 200+ Technology and Scientific Presentations
Connect with Attendees Using CHI’s Intro-Net
Participate in the Poster Competition
Choose from 14 Pre-Conference Workshops
See the Winners of these 2017 Awards:
Best of Show
View Novel Technologies and Solutions in the Expansive Exhibit Hall
Sequence Speaking Topic = The Path to Easier GXP Compliance
Science in the Age of Experience May 15-18, 2017 / Chicago, IL
Join us in Chicago for the 2017 Science in the Age of Experience, BIOVIA’s Customer User Group Meeting. The event will be held May 15-18, 2017 at the Hyatt Chicago McCormick Place. Building upon the success of last year’s inaugural event, this year’s conference will be larger than ever, with tracks and sessions featuring BIOVIA product experts, customers and industry thought leaders. The event will also feature presenters from SIMULIA, GEOVIA and other Dassault Systèmes brands. The week offers four days of proven best practices, hands-on training workshops and previews of the latest releases of BIOVIA products and services including integration with other solutions. There will be ample opportunities for networking with your industry colleagues and with BIOVIA and Dassault Systèmes experts. Science in the Age of Experience is not to be missed.