{"id":83564,"date":"2026-04-01T16:03:10","date_gmt":"2026-04-01T16:03:10","guid":{"rendered":"https:\/\/teeptrak.com\/interphex-2026-dates-exhibitors-pharma-manufacturers\/"},"modified":"2026-04-01T16:03:15","modified_gmt":"2026-04-01T16:03:15","slug":"interphex-2026-dates-exhibitors-pharma-manufacturers","status":"publish","type":"post","link":"https:\/\/teeptrak.com\/en\/interphex-2026-dates-exhibitors-pharma-manufacturers\/","title":{"rendered":"INTERPHEX 2026: Dates, Exhibitors and What Pharma Manufacturers Need to Know"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; _builder_version=&#8221;4.27&#8243;][et_pb_row][et_pb_column type=&#8221;4_4&#8243;][et_pb_text]<\/p>\n<p><script type=\"application\/ld+json\">\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"BlogPosting\",\n  \"headline\": \"INTERPHEX 2026: Dates, Exhibitors and What Pharma Manufacturers Need to Know\",\n  \"description\": \"INTERPHEX 2026 complete guide: dates, New York venue, top exhibitors, registration costs and how pharma manufacturers can maximize their visit ROI.\",\n  \"author\": {\n    \"@type\": \"Organization\",\n    \"name\": \"TeepTrak\"\n  },\n  \"publisher\": {\n    \"@type\": \"Organization\",\n    \"name\": \"TeepTrak\",\n    \"logo\": {\n      \"@type\": \"ImageObject\",\n      \"url\": \"https:\/\/teeptrak.com\/logo.png\"\n    }\n  },\n  \"datePublished\": \"2024-12-19\",\n  \"dateModified\": \"2024-12-19\",\n  \"mainEntityOfPage\": {\n    \"@type\": \"WebPage\",\n    \"@id\": \"https:\/\/teeptrak.com\/en\/interphex-2026-dates-exhibitors-pharma-manufacturers\/\"\n  },\n  \"keywords\": \"interphex 2026, pharmaceutical manufacturing, FDA compliance, OEE monitoring, pharma equipment\"\n}\n<\/script><\/p>\n<p><script type=\"application\/ld+json\">\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"When and where will INTERPHEX 2026 take place?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"INTERPHEX 2026 is expected to take place in April 2026 at the Jacob K. Javits Convention Center in New York City. The exact dates will be announced by Informa Markets closer to the event.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"How much does INTERPHEX 2026 registration cost?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"General exhibition floor admission typically costs $50-100, while conference passes with educational sessions range from $800-2000+. Early bird discounts are usually available.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What types of exhibitors will be at INTERPHEX 2026?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"INTERPHEX 2026 will feature pharmaceutical manufacturing equipment suppliers, bioprocessing companies, cleanroom technology providers, packaging and serialization solution vendors, IoT monitoring systems, laboratory instruments, regulatory compliance software, and API manufacturers.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Why is OEE monitoring important in pharmaceutical manufacturing?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"OEE monitoring is critical for FDA compliance, batch record integrity, and equipment qualification. Average pharma plant OEE ranges from 55-65%, significantly below world-class 85% benchmarks, indicating substantial improvement opportunities.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"How can IoT solutions comply with FDA 21 CFR Part 11 requirements?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"FDA 21 CFR Part 11 compliant IoT systems must provide electronic signature capabilities, audit trails, data integrity controls, and secure data storage. Solutions must validate data authenticity and prevent unauthorized modifications.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is the typical deployment time for IoT monitoring in pharma plants?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Modern IoT monitoring systems can be deployed in approximately 30 minutes per machine without interrupting production. The installation process involves non-invasive sensors that monitor equipment performance in real-time.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"How should pharmaceutical manufacturers prepare for INTERPHEX 2026?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Manufacturers should define their top 3 manufacturing challenges, research target exhibitors by problem categories, prepare ROI-focused questions about deployment time, compliance features, and system integration capabilities before attending.\"\n      }\n    }\n  ]\n}\n<\/script><\/p>\n<h1>INTERPHEX 2026: Dates, Exhibitors and What Pharma Manufacturers Need to Know<\/h1>\n<p>INTERPHEX stands as the premier pharmaceutical manufacturing exhibition in the Americas, attracting industry leaders, equipment manufacturers, and technology providers to New York City annually. The 2026 edition promises to be particularly significant as pharmaceutical manufacturers face mounting pressure to improve operational efficiency while maintaining strict regulatory compliance. With FDA regulations becoming increasingly stringent and global supply chain complexities intensifying, manufacturers who attend INTERPHEX 2026 will gain access to cutting-edge technologies, networking opportunities, and strategic insights that can transform their operations. The show serves as a crucial platform for discovering solutions that address the industry&#8217;s most pressing challenges, from serialization compliance to real-time monitoring systems that ensure product quality and regulatory adherence.<\/p>\n<h2>What is INTERPHEX?<\/h2>\n<p>The International Pharmaceutical Expo, commonly known as INTERPHEX, represents the pharmaceutical manufacturing industry&#8217;s most comprehensive trade show in North America. Organized annually by Informa Markets at the Jacob K. Javits Convention Center in New York City, this exhibition has evolved into an essential gathering point for pharmaceutical and biopharmaceutical professionals seeking advanced manufacturing solutions.<\/p>\n<p>INTERPHEX typically attracts over 10,000 attendees from across the global pharmaceutical ecosystem, including manufacturing executives, plant managers, quality assurance directors, regulatory affairs professionals, and procurement specialists. The exhibition floor hosts more than 500 exhibitors showcasing the latest innovations in pharmaceutical manufacturing equipment, bioprocessing technology, packaging solutions, and regulatory compliance systems.<\/p>\n<p>The show&#8217;s focus extends beyond traditional equipment displays to encompass critical industry themes such as serialization compliance, continuous manufacturing processes, advanced analytics, and digital transformation initiatives. Educational conference sessions complement the exhibition, featuring presentations from FDA representatives, industry thought leaders, and pharmaceutical manufacturing experts who share insights on regulatory changes, best practices, and emerging technologies.<\/p>\n<p>INTERPHEX serves multiple industry segments, including small molecule pharmaceutical manufacturing, biopharmaceutical production, contract manufacturing organizations (CMOs), and API manufacturers. The exhibition&#8217;s comprehensive scope makes it an invaluable resource for professionals seeking to understand market trends, evaluate new technologies, and establish strategic partnerships within the pharmaceutical manufacturing ecosystem.<\/p>\n<h2>INTERPHEX 2026 Key Dates and Logistics<\/h2>\n<p>INTERPHEX 2026 is expected to follow the traditional April scheduling pattern, taking place at the Jacob K. Javits Convention Center in New York City. While Informa Markets has not yet announced the exact dates, the show typically runs for three days during the second or third week of April, allowing optimal timing for industry professionals to attend without conflicting with major pharmaceutical conferences or regulatory deadlines.<\/p>\n<p>The Jacob K. Javits Convention Center, located on Manhattan&#8217;s West Side, provides 760,000 square feet of exhibition space across multiple floors. The facility&#8217;s modern infrastructure supports the complex requirements of pharmaceutical equipment demonstrations, including specialized power, compressed air, and environmental controls necessary for cleanroom technology displays and bioprocessing equipment operation.<\/p>\n<p>Registration costs for INTERPHEX 2026 are expected to align with previous years&#8217; pricing structure. General admission to the exhibition floor typically ranges from $50-100 for standard registration, with early bird discounts available for advance registrations. Comprehensive conference passes, which include access to educational sessions, networking events, and premium content, generally cost between $800-2000+ depending on the package selected.<\/p>\n<p>The floor plan traditionally allocates distinct zones for different technology categories, enabling attendees to navigate efficiently between related exhibitors. The bioprocessing pavilion, cleanroom technology section, and packaging equipment areas maintain consistent locations to facilitate visitor planning and maximize networking opportunities within specific technology segments.<\/p>\n<p>INTERPHEX 2026 will be co-located with the Healthcare Businesswomen&#8217;s Association (HBA) Annual Conference, creating additional networking opportunities and expanded educational programming. The international attendance profile typically includes representatives from European, Asian, and Latin American pharmaceutical companies, providing global perspectives on manufacturing challenges and regulatory requirements.<\/p>\n<h2>Top Exhibitor Categories at INTERPHEX 2026<\/h2>\n<p><strong>Pharmaceutical Manufacturing Equipment Suppliers<\/strong> represent the largest exhibitor category, showcasing tablet presses, capsule filling machines, granulation equipment, coating systems, and fluid bed dryers. Major manufacturers like GEA Group, Bosch Packaging Technology, and IMA demonstrate equipment capable of handling high-volume production while maintaining GMP compliance. These exhibitors typically present case studies showing throughput improvements, quality enhancements, and validation support services.<\/p>\n<p><strong>Bioprocessing and Upstream\/Downstream Processing<\/strong> companies focus on bioreactor systems, chromatography equipment, filtration technologies, and purification systems. Companies such as Sartorius, Merck KGaA, and Cytiva showcase single-use technologies, continuous bioprocessing solutions, and advanced control systems that enable flexible manufacturing approaches. This category addresses the growing demand for biologics production and personalized medicine manufacturing capabilities.<\/p>\n<p><strong>Cleanroom Technology and Contamination Control<\/strong> exhibitors present HEPA filtration systems, air handling units, environmental monitoring equipment, and personnel decontamination solutions. Companies like Terra Universal, Particle Measuring Systems, and Lighthouse Worldwide Solutions demonstrate technologies that maintain ISO 14644 cleanroom standards while optimizing energy consumption and operational efficiency.<\/p>\n<p><strong>Packaging and Serialization Solutions<\/strong> have gained prominence due to Drug Supply Chain Security Act (DSCSA) requirements and global serialization mandates. Exhibitors including Marchesini Group, K\u00f6rber Pharma, and Antares Vision showcase track-and-trace systems, aggregation solutions, and packaging line integration technologies that ensure regulatory compliance while maintaining production throughput.<\/p>\n<p><strong>IoT Monitoring and MES Systems<\/strong> represent a rapidly growing category addressing the industry&#8217;s digital transformation needs. TeepTrak positions within this segment, demonstrating how IoT sensors and real-time monitoring systems provide FDA 21 CFR Part 11 compliant data collection, OEE measurement, and predictive maintenance capabilities. This technology category appeals to manufacturers seeking to improve operational visibility and reduce unplanned downtime.<\/p>\n<p><strong>Laboratory Analytical Instruments<\/strong> exhibitors present HPLC systems, mass spectrometers, dissolution testing equipment, and stability chambers essential for pharmaceutical quality control. Companies such as Agilent Technologies, Waters Corporation, and Thermo Fisher Scientific showcase automated testing solutions, data integrity features, and method development capabilities that accelerate product development timelines.<\/p>\n<p><strong>Regulatory Compliance and Validation Software<\/strong> providers focus on electronic batch records, document management systems, change control platforms, and audit trail solutions. These exhibitors address the pharmaceutical industry&#8217;s need for paperless manufacturing processes while maintaining comprehensive documentation required by FDA, EMA, and other regulatory authorities.<\/p>\n<p><strong>API and Drug Substance Manufacturing<\/strong> companies showcase reaction systems, crystallization equipment, drying technologies, and containment solutions for active pharmaceutical ingredient production. This category serves both captive API manufacturers and contract development and manufacturing organizations (CDMOs) requiring flexible, scalable production capabilities.<\/p>\n<h2>How to Prepare Your Visit for Maximum ROI<\/h2>\n<p>Strategic preparation significantly impacts the value pharmaceutical manufacturers derive from INTERPHEX 2026 attendance. The most successful visitors approach the exhibition with clearly defined objectives, targeted exhibitor lists, and prepared evaluation criteria that align with their operational challenges and strategic goals.<\/p>\n<p>Begin preparation by identifying your top three manufacturing challenges, whether they involve regulatory compliance gaps, equipment reliability issues, capacity constraints, or quality control inefficiencies. Document current performance metrics, including OEE percentages, deviation rates, batch failure frequencies, and maintenance costs. This baseline data enables meaningful discussions with exhibitors and facilitates accurate ROI calculations for potential technology investments.<\/p>\n<p>Research exhibitor categories by problem rather than by technology type. If unplanned downtime represents your primary challenge, focus on predictive maintenance solutions, real-time monitoring systems, and equipment reliability technologies rather than limiting your search to traditional maintenance vendors. This problem-centric approach often reveals innovative solutions from unexpected sources.<\/p>\n<p>Prepare specific ROI-focused questions for each targeted exhibitor: What is the typical deployment timeline? How does the solution ensure FDA 21 CFR Part 11 compliance? What integration capabilities exist with current MES, ERP, or historian systems? Can the vendor provide pharmaceutical industry references and documented performance improvements? What validation support is included in the implementation package?<\/p>\n<p>A concrete case study illustrates the preparation impact: A pharmaceutical plant manager attended INTERPHEX 2025 without specific objectives, spending three days touring booths randomly and collecting generic brochures. The result was information overload with no actionable outcomes. In contrast, a peer from the same company attended with documented challenges, targeted exhibitor appointments, and prepared questions. This strategic approach resulted in identifying three viable solutions, scheduling post-show evaluations, and ultimately implementing a monitoring system that improved OEE by 8 percentage points within six months.<\/p>\n<p>Schedule exhibitor meetings in advance through the official INTERPHEX 2026 website or mobile application. Many suppliers offer exclusive show pricing, extended evaluation periods, or implementation incentives available only to exhibition attendees. Pre-scheduled appointments ensure access to senior technical staff and decision-makers who may not be available for unscheduled visits during peak show hours.<\/p>\n<h2>OEE and IoT Monitoring in Pharma Manufacturing<\/h2>\n<p>Overall Equipment Effectiveness (OEE) measurement has become increasingly critical in pharmaceutical manufacturing due to FDA requirements for batch record integrity, equipment qualification protocols (IQ\/OQ\/PQ), and continuous process verification initiatives. The pharmaceutical industry&#8217;s unique regulatory environment demands comprehensive documentation of equipment performance, making real-time monitoring systems essential for compliance and operational excellence.<\/p>\n<p>Current pharmaceutical industry benchmarks reveal significant improvement opportunities, with average plant OEE ranging from 55-65% compared to world-class manufacturing standards of 85% or higher. This performance gap represents substantial untapped potential in production capacity, cost reduction, and regulatory compliance enhancement. Low OEE scores in pharmaceutical manufacturing typically result from extended changeover times between products, equipment failures during critical production phases, quality-related production stops, and regulatory-required cleaning and validation procedures.<\/p>\n<p>FDA 21 CFR Part 11 compliance requirements add complexity to pharmaceutical monitoring systems, mandating electronic signature capabilities, audit trails, data integrity controls, and secure data storage. Traditional paper-based data collection methods cannot meet these electronic records requirements, driving pharmaceutical manufacturers toward validated IoT monitoring solutions that automatically capture performance data while maintaining regulatory compliance.<\/p>\n<p>Modern IoT sensors deploy on pharmaceutical equipment with minimal production disruption, typically requiring approximately 30 minutes per machine for installation. Non-invasive sensor technologies monitor critical parameters including equipment cycle times, temperature variations, pressure fluctuations, vibration patterns, and energy consumption without interfering with product contact surfaces or compromising sterile environments.<\/p>\n<p>TeepTrak IoT monitoring system demonstrates proven results in pharmaceutical environments, with one client achieving an 11-point OEE improvement within five months of implementation. The same facility experienced a 35% reduction in unplanned downtime through predictive maintenance alerts and real-time equipment health monitoring. These improvements translated to increased production capacity equivalent to adding a third production shift without additional labor or equipment investments.<\/p>\n<p>The system&#8217;s FDA 21 CFR Part 11 compliant data collection automatically generates electronic batch records, equipment utilization reports, and maintenance documentation required for regulatory submissions. Integration capabilities with existing MES, ERP, and quality management systems ensure seamless data flow while maintaining data integrity throughout the pharmaceutical manufacturing process.<\/p>\n<p>Real-time visibility into equipment performance enables pharmaceutical manufacturers to identify inefficiencies, optimize maintenance schedules, and implement continuous improvement initiatives that enhance both operational performance and regulatory compliance. The combination of automated data collection, advanced analytics, and predictive insights transforms traditional reactive maintenance approaches into proactive strategies that maximize equipment reliability and production consistency.<\/p>\n<h2>TeepTrak at INTERPHEX Context<\/h2>\n<p>IoT monitoring solutions resonate strongly with INTERPHEX audiences due to the pharmaceutical industry&#8217;s increasing focus on digital transformation, regulatory compliance automation, and operational efficiency improvement. Pharmaceutical manufacturers attending INTERPHEX 2026 face mounting pressure to modernize legacy systems while maintaining strict quality standards and regulatory adherence.<\/p>\n<p>TeepTrak has established a proven track record across 450+ factories in 30 countries, with deployments spanning pharmaceutical, biopharmaceutical, defense, and high-technology manufacturing sectors. The solution&#8217;s versatility and regulatory compliance capabilities make it particularly well-suited for pharmaceutical applications where data integrity, audit trails, and validation documentation represent critical requirements.<\/p>\n<p>Notable client references include Thales and Safran, both operating in highly regulated defense and aerospace industries that demand similar quality standards and documentation rigor as pharmaceutical manufacturing. These references demonstrate TeepTrak&#8217;s capability to meet stringent regulatory requirements while delivering measurable operational improvements in complex manufacturing environments.<\/p>\n<p>The system&#8217;s FDA 21 CFR Part 11 compliance features address pharmaceutical manufacturers&#8217; most pressing regulatory concerns, providing electronic signature capabilities, comprehensive audit trails, and secure data storage that meets FDA validation requirements. This compliance foundation eliminates the lengthy and costly validation processes typically associated with implementing new manufacturing systems in pharmaceutical facilities.<\/p>\n<p>Serialization data integration capabilities enable pharmaceutical manufacturers to connect real-time production monitoring with track-and-trace systems, creating comprehensive visibility across the entire manufacturing process. This integration supports DSCSA compliance requirements while providing operational insights that improve production planning, quality control, and supply chain visibility.<\/p>\n<p>The <a href=\"https:\/\/teeptrak.com\/en\/solution\/\">TeepTrak solution<\/a> addresses multiple pharmaceutical manufacturing challenges simultaneously, including OEE optimization, predictive maintenance implementation, regulatory compliance automation, and quality system enhancement. This comprehensive approach resonates with pharmaceutical executives seeking integrated solutions rather than point technologies that require complex system integration efforts.<\/p>\n<p>Manufacturing professionals attending INTERPHEX 2026 will find TeepTrak&#8217;s rapid deployment capabilities particularly attractive, given the pharmaceutical industry&#8217;s preference for minimal production disruption during system implementations. The 30-minute per machine installation process, combined with immediate data availability and validated compliance features, provides pharmaceutical manufacturers with a low-risk pathway to digital transformation benefits.<\/p>\n<p>Case studies and performance data from pharmaceutical <a href=\"https:\/\/teeptrak.com\/en\/clients\/\">clients<\/a> demonstrate concrete results that INTERPHEX attendees can relate to their operational challenges. The documented OEE improvements, downtime reductions, and maintenance cost savings provide quantifiable evidence of ROI potential that supports executive decision-making processes in pharmaceutical organizations.<\/p>\n<h2>Frequently Asked Questions<\/h2>\n<p><strong>When and where will INTERPHEX 2026 take place?<\/strong><\/p>\n<p>INTERPHEX 2026 is expected to take place in April 2026 at the Jacob K. Javits Convention Center in New York City. The exact dates will be announced by Informa Markets closer to the event, following the traditional three-day format that has proven successful for attendee engagement and exhibitor participation.<\/p>\n<p><strong>How much does INTERPHEX 2026 registration cost?<\/strong><\/p>\n<p>General exhibition floor admission typically costs $50-100 for standard registration, while comprehensive conference passes with educational sessions range from $800-2000+ depending on the package selected. Early bird discounts are usually available for advance registrations, and group rates may apply for multiple attendees from the same organization.<\/p>\n<p><strong>What types of exhibitors will be at INTERPHEX 2026?<\/strong><\/p>\n<p>INTERPHEX 2026 will feature pharmaceutical manufacturing equipment suppliers, bioprocessing companies, cleanroom technology providers, packaging and serialization solution vendors, IoT monitoring systems, laboratory analytical instruments, regulatory compliance software providers, and API manufacturers representing the complete pharmaceutical manufacturing ecosystem.<\/p>\n<p><strong>Why is OEE monitoring important in pharmaceutical manufacturing?<\/strong><\/p>\n<p>OEE monitoring is critical for FDA compliance, batch record integrity, and equipment qualification requirements. Average pharmaceutical plant OEE ranges from 55-65%, significantly below world-class benchmarks of 85%, indicating substantial improvement opportunities through real-time monitoring and predictive maintenance implementation.<\/p>\n<p><strong>How can IoT solutions comply with FDA 21 CFR Part 11 requirements?<\/strong><\/p>\n<p>FDA 21 CFR Part 11 compliant IoT systems must provide electronic signature capabilities, comprehensive audit trails, data integrity controls, and secure data storage. Solutions must validate data authenticity, prevent unauthorized modifications, and maintain complete documentation of all system interactions and data changes.<\/p>\n<p><strong>What is the typical deployment time for IoT monitoring in pharmaceutical plants?<\/strong><\/p>\n<p>Modern IoT monitoring systems can be deployed in approximately 30 minutes per machine without interrupting production operations. The installation process involves non-invasive sensors that monitor equipment performance in real-time while maintaining sterile environments and product contact surface integrity.<\/p>\n<p><strong>How should pharmaceutical manufacturers prepare for INTERPHEX 2026?<\/strong><\/p>\n<p>Manufacturers should define their top three manufacturing challenges, research target exhibitors by problem categories rather than technology types, and prepare ROI-focused questions about deployment timelines, compliance features, system integration capabilities, and pharmaceutical industry references before attending the exhibition.<\/p>\n<p style=\"text-align:center;margin-top:40px;\"><a href=\"https:\/\/teeptrak.com\/en\/demo\/\" style=\"background-color:#EB352C;color:#ffffff;padding:16px 32px;border-radius:4px;text-decoration:none;font-weight:bold;font-size:16px;\">Schedule Your INTERPHEX 2026 Meeting<\/a><\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; _builder_version=&#8221;4.27&#8243;][et_pb_row][et_pb_column type=&#8221;4_4&#8243;][et_pb_text] INTERPHEX 2026: Dates, Exhibitors and What Pharma Manufacturers Need to Know INTERPHEX stands as the premier pharmaceutical manufacturing exhibition in the Americas, attracting industry leaders, equipment manufacturers, and technology providers to New York City annually. The 2026 edition promises to be particularly significant as pharmaceutical manufacturers face mounting pressure to improve [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":83558,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","ai_seo_title":"","ai_meta_description":"","ai_focus_keyword":"","footnotes":""},"categories":[9],"tags":[],"class_list":["post-83564","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-non-classifiee"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>INTERPHEX 2026: Dates, Exhibitors and What Pharma Manufacturers Need to Know - TEEPTRAK - Connect to your industrial potential<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/teeptrak.com\/en\/interphex-2026-dates-exhibitors-pharma-manufacturers\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"INTERPHEX 2026: Dates, Exhibitors and What Pharma Manufacturers Need to Know - TEEPTRAK - Connect to your industrial potential\" \/>\n<meta property=\"og:description\" content=\"[et_pb_section fb_built=&#8221;1&#8243; _builder_version=&#8221;4.27&#8243;][et_pb_row][et_pb_column type=&#8221;4_4&#8243;][et_pb_text] INTERPHEX 2026: Dates, Exhibitors and What Pharma Manufacturers Need to Know INTERPHEX stands as the premier pharmaceutical manufacturing exhibition in the Americas, attracting industry leaders, equipment manufacturers, and technology providers to New York City annually. 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