GMP & QP Services from Clinical Development to Commercial Supply. Independent EU Qualified Person expertise across the full product lifecycle.
FAREVA
Farera as a CDMO is providing a large service offer as sterile injectable and high potent, biological drug, conventionnal product, medial devices, foods supllements and probiotics as well as Drug substance manufacturing of recombinant protein, Andibody Dug Conjugason (ADC) with the associated Fill& Finish | FAREVA is a leading global pharmaceutical CDMO with industry leading capabilities in the development and manufacturing of a large range of Drug Products and Active Pharmaceutical Ingredients (APIs). FAREVA employs 13,000 people distributed in 41 production sites located in 13 countries in EMEA and the Americas. 16 of the FAREVA sites are dedicated to pharmaceutical activities. FAREVA’s API division has operations in 3 European sites located in France and Germany. | Fareva is a leading global pharmaceutical CDMO with a network of 16 manufacturing sites and 3 development sites throughout EMEA and the Americans. We offer comprehensive drug product and API services, including formulation development, clinical manufacturing, scale-up, and commercial manufacturing of small and large molecules. Our capabilities cover a wide range of dosage forms, such as OTC products, oral solid doses, non-sterile liquids and solids, ophthalmics, as well as sterile fill/finish and lyophilized presentations. In addition, our facilities have extensive expertise in secondary packaging, enabling us to serve as a fully integrated partner for our clients’ end-to-end pharmaceutical needs.
EFOR Group
Founded in 2013, Efor Group is a leading international player in quality and compliance for the Life Sciences industry. With over 3,000 employees across 18 countries, Efor supports leading pharmaceutical, biotech, and medtech companies in securing their manufacturing operations through its expertise in CQV, quality management, and regulatory compliance, while accelerating the delivery of innovative therapies to market. Our mission: to remove technical and regulatory barriers, enabling faster access to innovation while ensuring the highest standards of safety and reliability. Committed to its founding values, Efor fully integrates social and environmental responsibility into its business model and drives sustainable growth built on excellence, commitment, and teamwork. Through its international expansion, the Group aims to establish itself as a global reference in Life Sciences consulting, placing people, health, and safety at the heart of everything it does.
Ecolab Life Sciences
Ecolab’s Purolite™ Resins receive continued investment from Ecolab to support development, production, and customer support. We have one of the industry’s largest technically trained sales teams in ion exchange and specialty resin technology, backed by five Research and Development centers, nine application labs and five production facilities. With our ability to quickly respond, supply, and develop, we can solve your application challenges and optimize your system. Ecolab’s Life Sciences division is dedicated to developing the best possible products and services to support our customers in the pharmaceutical industry. Our comprehensive solutions and technical expertise are focused on cleaning, sanitization and contamination control, all while ensuring safety, compliance and operational efficiency. Our strategy is to stay focused on two core areas: Global Trends and Regulatory Changes that impact your operations, and develop solutions to keep you on the cutting edge. | Ecolab Life Sciences is a segment of Ecolab and a global leader in technologies and services designed to enhance productivity, reduce costs, and accelerate the development of critical medicines. Leveraging over a century of innovation, Ecolab Life Sciences provides comprehensive solutions and expert guidance across bio-decontamination, drug purification, active pharmaceutical ingredients (APIs) and excipients. With a strong commitment to ensuring safety, compliance, and operational efficiency, Ecolab Life Sciences partners with organizations to support their mission of advancing health and wellbeing worldwide.
CRQA
CRQA: Your Trusted GxP Compliance and Regulatory Consulting Partner Company: CRQA (Compliance, Regulatory & Quality Assurance) Headquarters: Noida, Uttar Pradesh, India (Office No. 602, 6th Floor, Tower B, B8 Noida One, Sector 62) Website: www.crqa.in Contact: bd@crqa.in | +91 98100 68241 Tagline: GxP Compliance: We have got you covered Who We Are CRQA is an independent, specialized auditing and regulatory consulting organization headquartered in New Delhi/Noida, India. Unlike large contract research organizations (CROs) that offer quality assurance as an add-on, CRQA was built exclusively around GxP compliance — making regulatory excellence our sole focus, not a side offering. Registered with Dun & Bradstreet, ISO 13485 & ISO 9011:2015 certified, and recognized as an MSME, CRQA has positioned itself as a credible and conflict-free compliance partner for pharmaceutical companies, biotechnology firms, clinical research organizations, medical device manufacturers, and healthcare institutions worldwide. Global Reach CRQA operates across more than 60 countries and delivers its services in 30 languages, making it one of the most geographically diverse independent GxP auditing firms in the world. Our network of Auditors spans: • Asia: India, Japan, China, Southeast Asia, including major Indian cities — New Delhi NCR, Noida, Gurgaon, Mumbai, Pune, Bangalore, Chennai, Hyderabad, Kolkata, Ahmedabad, Vadodara • Americas: United States, Latin America • Europe: EU countries, UK • Middle East & Africa • Australia & Oceania This wide geographical presence enables us to deploy region-based auditors who understand local regulatory environments — reducing travel costs and turnaround time for our clients. Why CRQA? — The Value Proposition CRQA was founded to address a critical gap in the pharmaceutical services industry: the absence of a dedicated, independent auditing agency free from conflicts of interest. Key advantages of working with CRQA: ✔ No conflict of interest — CRQA is purely an auditing and consulting firm; we do not run clinical trials or offer CRO services, ensuring full objectivity in every audit. ✔ Specialized expertise — Our auditors are seasoned professionals with deep GxP knowledge, offering a level of focus that generalist CROs cannot match. ✔ Cost efficiency — With locally based auditors across 60+ countries, clients benefit from significant cost savings on travel and logistics. ✔ Better sponsor–CRO relationships — By outsourcing audits to CRQA rather than using competitor CROs, sponsors can maintain neutral, healthy vendor relationships. ✔ Holistic compliance perspective — Our external auditors provide an unbiased, big-picture view of a client’s systems, identifying gaps and improvement opportunities that internal teams may overlook. Services Portfolio CRQA provides a comprehensive suite of GxP auditing and regulatory consulting services: Clinical & Research Compliance • GCP (Good Clinical Practice) Audits and Services • GCP Consultancy • Mock Inspections • BA/BE (Bioavailability/Bioequivalence) CRO Audits • Remote GCP and Pharmacovigilance Audits • Vendor Audits • Study Audits Manufacturing & Distribution Quality • GMP (Good Manufacturing Practice) Audits and Services • GDP (Good Distribution Practice) Compliance • GLP/GCLP (Good Laboratory/Clinical Laboratory Practice) Audits • Pharmaceutical Quality Management Services Pharmacovigilance & Drug Safety • Pharmacovigilance Audits • QPPV (Qualified Person for Pharmacovigilance) Services • Global Pharmacovigilance Outsourcing Services Medical Devices • Medical Device Regulatory Audits and Consulting • ISO 13485 Quality Management System Support Regulatory Affairs & Strategy • Regulatory Pathway Consulting Services • Global Pharmaceutical Outsourcing Services • Dossier Submission Support (Feasibility to Filing) • Qualified Person (QP) Services in Europe Technology & Systems Compliance • Computer System Validation (CSV) • Compliance Training on 21 CFR Part 11 Quality Systems & SOPs • Quality Management and Compliance Systems • SOPs Development and Review Training & Education • Online Training and Workshops • Ethics Committee / IRB Training • Compliance Training Programs Key Clients CRQA has earned the trust of a diverse global clientele, including recognized names across pharma, biotech, medical devices, and healthcare and have worked with wide range of pharma, biopharma and medical device clients from USA, Europe, India. Certifications & Recognition • D-U-N-S Registered (Dun & Bradstreet Verified) • ISO 13485 Certified (Medical Devices Quality Management Systems) • ISO 9001 : 2015 • MSME Recognized (Government of India) Our Differentiator at BIO USA At a conference where partnerships are forged and life sciences innovation meets business strategy, CRQA stands out as the go-to independent partner for: • Pharma and biotech companies entering new markets who need local regulatory audit support • CROs and sponsors seeking objective, third-party GxP compliance evaluations • Medical device companies needing ISO 13485 audits and regulatory consulting • Global life sciences firms looking for cost-effective, scalable compliance solutions across multiple geographies Whether you are preparing for an FDA, EMA, or CDSCO inspection, building your quality management infrastructure, or seeking ongoing pharmacovigilance oversight — CRQA delivers expert, independent, and conflict-free compliance support. Connect With Us at BIO USA kshahani@crqa.in +91 98100 68241 www.crqa.in LinkedIn: CRQA India CRQA — GxP Compliance: We Have Got You Covered.
BrevisRefero
BrevisRefero, in partnership with the educational platform BrickMMO, is pleased to be showcasing an ‘Interactive Biologics CDMO Facility Constructed Exclusively from LEGO(R) Bricks’ at it’s booth (1313) at BIO2024. Join us at our booth for an immersive and educational look at the biologics manufacturing like never before! BrevisRefero is a collection of biologics professionals who share a common goal – to improve and support the management of biologics programs from concept to development, GMP manufacturing and into clinical trials for the benefit of patient and sponsor alike. Pulling from more than 100 years of collective technical biotech consulting experience, we work closely with our clients to develop realistic technical and strategic solutions to support the execution and delivery of biologics programs. BrevisRefero also hosts an RFP outsource management platform called RFP>Navigator(R) that simplifies and accelerates Sponsor’s selection of their CDMO partners. | BrevisRefero Corporation is a team of biopharma professionals with a collective 100 years of biotechnology experience who assist Innovator companies to develop and manufacture their large-molecule biologics for clinical trials and commercial markets. The company assists Innovators by partnering with them at the target molecule post discovery stage and walking with them through their product development journey. Ground-level assistive support is provided in all technical aspects of drug development – from analytical methods and process development, through to scale-up and GMP manufacturing, and every aspect in between supporting their CMC program. Utilizing the deep-seated technical experience of BrevisRefero’s full-time consultants, we have developed innovative world-class online technology tools. Our award-winning commercial product RFP>Navigator®as well as our newly developed BioBudget Champion(TM) tool help propel the biopharma industry forward. Whether it is through our technical knowledge, or its application, BrevisRefero is driven to enable Innovators to succeed in their product development journey.
BIO Business Solutions®
BIO Business Solutions is the largest cost-savings purchasing program for the life sciences industry, operated by BIO. We pool the purchasing power of thousands of life sciences companies to negotiate for exclusive pricing and favorable terms on business-critical products, like lab supplies, regulatory services, HR and much more. BIO helped 4,700 life science companies save over $705 million last year alone. | BIO Business Solutions is the largest cost-savings program for the life sciences industry, operated by BIO. We pool the purchasing power of thousands of life science companies to negotiate for exclusive pricing and favorable terms on business-critical products, like lab supplies, cleanroom services, HR and much more. Every year, BIO helps nearly 5,000 companies save over $700 million. | BIO Business Solutions is the largest cost savings program for the life sciences industry, operated by BIO. BIO Business Solutions negotiates significant volume-based discounts, favorable terms, and other benefits on products and services with industry leading suppliers on behalf of BIO members and the members of state and regional biotech associations. Learn more at bio.org/save.
Benilight
Illuminating the Future of Brain Health: Benilight at BioUSA 2026 The Vision: Beyond Light, Toward Neural Recovery In a world grappling with a growing mental health crisis, Benilight is redefining the boundaries of non-invasive therapy. We don’t just provide devices; we provide a Neural Recovery Ecosystem. At BioUSA 2026, we are proud to unveil the next evolution of our flagship technology: the iLED Pro, now integrated with an AI-powered Medical Doctor App, specifically targeting Post-Traumatic Stress Disorder (PTSD). Core Innovation: The iLED Pro & AI Synergy The iLED Pro is an FDA-listed, professional-grade photobiomodulation (PBM) device. While it has already set industry standards for pain management and tissue recovery, our focus has shifted toward the final frontier: The Brain. Triple-Wavelength Precision: Utilizing a combination of 660nm (Red), 850nm (NIR), and 940nm (NIR), the iLED Pro penetrates deep into cortical tissues to stimulate mitochondrial function and ATP production. Ethical Engineering: Our flexible LED pads are built for the rigors of clinical and home use, tested to withstand over 300,000 bends without losing intensity or integrity. The AI Doctor Integration: Our new AI-driven application acts as a digital clinician. It monitors patient progress, optimizes light dosages based on neurological biofeedback, and provides real-time data to healthcare providers, making the iLED Pro a truly “smart” medical asset. The Indication: A New Hope for PTSD Post-Traumatic Stress Disorder remains one of the most difficult conditions to treat without heavy reliance on pharmaceuticals. Benilight is currently pursuing clinical evidence and regulatory pathways for a PTSD indication, leveraging PBM’s ability to: – Reduce Neuro-inflammation: Calming the physiological “storm” associated with trauma. – Enhance Connectivity: Improving functional connectivity in brain regions impacted by TBI and PTSD. – Optimize Sleep & Circadian Rhythms: Directly addressing the insomnia and night terrors that plague PTSD survivors. Strategic Opportunities for Partners We are at BioUSA to meet the visionaries who will help us scale this life-changing technology globally. Our Value Propositions : – Participation in a high-growth Digital Health firm bridging the gap between MedTech hardware and AI software. – Exclusive access to a versatile, FDA-listed device with a massive untapped market in mental health and sports medicine. – Collaborative opportunities to integrate our LED technology into broader telehealth platforms or specialized clinical chains. Why Visit the Benilight Booth? – Live Demos: Experience the soothing, deep-penetration technology of the iLED Pro firsthand. – The AI Interface: See how our AI App transforms a light therapy device into a sophisticated diagnostic and treatment tool. – Clinical Insights: Speak with our leadership team, including CEO Yosik Song and CTO Dr. Sungkyoo Lim, who brings over 30 years of light-science expertise to the table. Meet Us in San Diego – Event: Bio International Convention (BioUSA) 2026 – Location: San Diego Convention Center – Dates: June 22 – 25, 2026 – Focus: AI-Powered Photobiomodulation for PTSD & Brain Health | Benilight has developed LED medical devices and healthcare products utilizing red LEDs and near-infrared (NIR) LEDs. Our company has conducted extensive research on the effects of LED light on the skin. These devices have been listed as Class II medical devices by the US FDA for pain relief and the enhancement of blood circulation.
Barrington James
Barrington James are an industry leading, global recruitment business that exclusively serves the Pharmaceutical, Biotechnology and Medical Device sectors. With offices all over the world and hundreds of specialists dedicated to sourcing exceptional talent, we have the capacity and capabilities to deliver world-class recruitment solutions to Life Science companies of all sizes.