COVID-19 Vaccine Logistics Chain Reliability and Compliance
Bureau Veritas , a world leader in testing, inspection, and certification, and OPTEL , a leading global provider of pharmaceutical supply chain traceability platforms, join forces to address the critical issue of reliability and traceability in COVID-19 vaccine logistics chains.
This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210106005697/en/
In the next few months, billions of doses of COVID-19 vaccines will need to be rapidly and safely administered to people around the world. The complexity of cold chain conditions, the timeliness of delivery as well as the need to mitigate risk of any deviation are identified as critical challenges for successful large-scale vaccination.
V-TRACE is an integrated solution designed to track and trace COVID-19 vaccines, while ensuring risk mitigation thanks to controls and inspections all along the logistics chain. V-TRACE provides a global control of the supply chain thanks to the local presence of inspectors in the field.
Didier Michaud-Daniel, CEO, Bureau Veritas, commented:
“The priority for all governments and private institutions is to ensure that vaccine doses are safe and secure. This means tracking and tracing vaccines along the supply chain. Bureau Veritas’ experience in independent inspections along the supply chain to control inventories, storage and logistics conditions complements OPTEL’s ability to provide real-time traceability information. By combining our respective expertise, we are able to provide a single solution to control and mitigate risk throughout the logistics chains. Building on almost 200 years of expertise in shaping trust between companies, governments and society at large, Bureau Veritas is proud to partner with OPTEL to ensure the health and safety of people around the world.”
Louis Roy, Founder and CEO, OPTEL Group, added:
“ The COVID-19 vaccine distribution is an unprecedented challenge for nations across the world. To successfully address this challenge, nations will need transparency at every level of the supply chain. This is precisely what OPTEL’s traceability platform has been built for, over the last three decades. OPTEL is proud to be joining forces with Bureau Veritas to bring complete visibility and certainty to the distribution of vaccines. As the leader in digital traceability, our mission is to use our technologies to create a better world. We know our traceability technologies combined with the expertise of Bureau Veritas can make a difference to overcome this historical challenge. ”
Thanks to this partnership, OPTEL and Bureau Veritas are able to offer a combined expertise that is unrivalled in the pharmaceutical industry and in supply chain assurance.
V-TRACE is a unique integrated solution providing Governments with:
- VISIBILITY to control their vaccine orders all along the logistics chain in one single control tower, ensuring the traceability of every batch of vaccines.
- COMPLIANCE of vaccine batches through verified collected information on storage and distribution conditions all along the logistics chain.
- ASSURANCE that their vaccines are well stored, transported and conserved, in particular assurance that cold chain requirements are met, with temperature verification performed by Bureau Veritas’ inspectors along the logistics chain.
About OPTEL Group
OPTEL is a leading global provider of traceability systems whose goal is to use its innovative technologies to build a better world through the Intelligent Supply Chain®.
OPTEL is the only company with the ability to offer true end-to-end traceability, providing actionable, granular data at every step of the supply chain—from raw materials to the consumer and beyond.
Founded in 1989, OPTEL is a Certified B Corporation headquartered in Canada, with facilities in India, Ireland and Brazil, as well as employees worldwide.
With more than 30 years of expertise and experience in the pharmaceutical supply chain, OPTEL is working with the world leading brands and tracking 15B items per year.
For more information, visit www.optelgroup.com.
About Bureau Veritas
Bureau Veritas is a world leader in laboratory testing, inspection and certification services. Created in 1828, the Group has more than 75,000 employees located in more than 1,500 offices and laboratories around the globe. Bureau Veritas helps its clients improve their performance by offering services and innovative solutions in order to ensure that their assets, products, infrastructure and processes meet standards and regulations in terms of quality, health and safety, environmental protection and social responsibility.
Bureau Veritas is also a global leader in supply chain assurance and COVID-19 hygiene protocol audits: with 70+ accreditations, 145,000+ certificates, a presence in 140+ countries, and recognized experience with governments, the group has supported its clients in the restart of their activities post COVID-19 lockdowns.
Bureau Veritas is listed on Euronext Paris and belongs to the Next 20 index.
Compartment A, ISIN code FR 0006174348, stock symbol: BVI.
For more information, visit www.bureauveritas.com, and follow us on Twitter (@bureauveritas) and LinkedIn.
|
|
Our information is certified with blockchain technology. Check that this press release is genuine at www.wiztrust.com. |
To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.
View source version on businesswire.com: https://www.businesswire.com/news/home/20210106005697/en/
Contact information
ANALYST/INVESTOR CONTACTS
Laurent Brunelle
+33 (0)1 55 24 76 09
laurent.brunelle@bureauveritas.com
Florent Chaix
+33 (0)1 55 24 77 80
florent.chaix@bureauveritas.com
MEDIA CONTACTS
Véronique Gielec
+33 (0)1 55 24 76 01
veronique.gielec@bureauveritas.com
Michèle Arcand
OPTEL Group
+1 418-261-9119
michele.arcand@optelgroup.com
DGM Conseil
+33 (0)1 40 70 11 89
thomasdeclimens@dgm-conseil.fr
quentin.hua@dgm-conseil.fr
About Business Wire
For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Takeda’s Zasocitinib Landmark Phase 3 Plaque Psoriasis Data Show Promise to Deliver Clear Skin in a Once-Daily Pill, Catalyzing a New Era of Treatment18.12.2025 10:00:00 EET | Press release
Takeda(TSE:4502/NYSE:TAK)today announced positive topline results for the two pivotal Phase 3randomized, multicenter, double-blind, placebo- and active comparator-controlled studies of zasocitinib (TAK-279), a next-generation, highly selective oral tyrosine kinase 2 (TYK2) inhibitor, in adults with moderate-to-severe plaque psoriasis (PsO). The studies demonstrated superiority of zasocitinib compared to placebo for the co-primary endpoints, static Physician Global Assessment (sPGA) 0/1 and Psoriasis Area and Severity Index (PASI) 75, at week 16, with a significantly greater PASI 75 response rate seen as early as week 4 and continuing to increase through week 24. The studies also met all 44 ranked secondary endpoints, including PASI 90, PASI 100 and sPGA 0 against placebo and apremilast, showing the potential of a convenient once-daily pill to deliver complete skin clearance for patients with PsO. “People living with psoriasis continue to seek safe, effective and fast-acting oral therap
DATROWAY ® Type II Variation Application Validated in the EU as First-Line Treatment for Patients with Metastatic Triple Negative Breast Cancer Who are Not Candidates for Immunotherapy18.12.2025 09:30:00 EET | Press release
The European Medicines Agency (EMA) has validated the Type II Variation marketing authorization application for DATROWAY® (datopotamab deruxtecan) as monotherapy for the first-line treatment of adult patients with unresectable or metastatic triple negative breast cancer (TNBC) who are not candidates for PD-1/PD-L1 inhibitor therapy. DATROWAY is a specifically engineered TROP2 directed DXd antibody drug conjugate (ADC) discovered by Daiichi Sankyo (TSE: 4568) and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca (LSE/STO/Nasdaq: AZN). The validation confirms the completion of the application and commences the scientific review process by the EMA’s Committee for Medicinal Products for Human Use. The application is based on data from the TROPION-Breast02 phase 3 trial presented in a late-breaking proffered paper session at the 2025 European Society for Medical Oncology (#ESMO25) Congress. In the trial, DATROWAY demonstrated statistically significant and clinical
Celltrion receives positive CHMP Opinion for SteQeyma™ (ustekinumab biosimilar) autoinjector18.12.2025 04:41:00 EET | Press release
Celltrion, Inc. today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion of autoinjector of SteQeyma™, a biosimilar to Stelara® (ustekinumab), for the treatment of plaque psoriasis, psoriatic arthritis (PsA) and Crohn’s disease (CD). The positive CHMP opinion is for SteQeyma autoinjector in 45mg/0.5mL and 90mg/1mL, expanding the currently approved SteQeyma™ presentation, which includes 45mg/0.5mL, 90mg/1mL in a pre-filled syringe and 45mg/0.5mL in a vial for subcutaneous injection, as well as 130mg/26mL concentrate for solution for intravenous infusion. “The new SteQeyma™ autoinjector brings together convenience and practical usability to meet the everyday challenges faced by patients living with chronic inflammatory diseases. The full range of our SteQeyma™ dosage forms and strengths, with the autoinjector now added, provides patients and healthcare professionals with more individualized treatm
Megaport Expands into India, Accelerating Global Growth with Extreme IX Acquisition18.12.2025 03:15:00 EET | Press release
Megaport Limited (ASX: MP1) (“Megaport”), the world’s leading Network as a Service (NaaS) provider, today announced the acquisition of Extreme IX,India’s leading Internet Exchange operator, from Extreme Labs, a Bulgaria-headquartered software and network engineering company that incubated the Extreme IX platform. The acquisition expands Megaport’s global platform into one of the world’s fastest-growing digital infrastructure markets and supports the Company’s strategy to deliver scalable, high-performance connectivity services across APAC. The acquisition establishes Megaport’s presence across seven Internet Exchanges in major Indian metros: Delhi, Kolkata, Hyderabad, Chennai, Bengaluru, Mumbai, and Pune, connecting 40+ data centres and more than 400 customers. It also accelerates Megaport’s planned market entry by nearly three years, while adding a seasoned in-country team spanning operations, support, sales, finance, and leadership to enable rapid integration and future growth. The E
IonQ and QuantumBasel Expand Long-Term Partnership in Next-Generation Quantum Systems17.12.2025 23:10:00 EET | Press release
IonQ (NYSE: IONQ), the world’s leading quantum company, today announced an expanded agreement with QuantumBasel, the quantum initiative of uptownBasel, Switzerland’s innovation campus. The extended contract grants QuantumBasel ownership of its existing IonQ Forte Enterprise system and secures ownership of a next-generation Tempo system. This new agreement brings the total deal value of the QuantumBasel and IonQ partnership to over $60 million and extends IonQ’s on-site presence in Switzerland four more years, continuing through 2029. QuantumBasel is IonQ’s official Innovation Center in Europe, serving as a hub for European industry, academia, and research institutions to explore practical quantum computing applications and access IonQ’s latest enterprise-grade systems. “Our extended partnership with QuantumBasel represents a cornerstone of IonQ’s global strategy,” said Niccolo de Masi, Chairman and CEO of IonQ. “QuantumBasel continues to be a critical innovation node for our company as
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom
