Expo

CPC Scientific
Founded in 2001, CPC Scientific is a trusted partner for leading pharmaceutical and biotechnology companies, as well as prestigious academic institutions worldwide. We specialize in the development and manufacturing of synthetic GMP peptides, oligonucleotides, and peptide-oligonucleotide conjugates (POCs). Our extensive portfolio includes custom and catalog research-grade products, tailored to meet the diverse needs of our clients.

In addition to custom solutions, CPC Scientific offers a diverse range of generic peptides used as APIs in treatments for diseases such as cancer, diabetes, obesity, and multiple sclerosis. Our state-of-the-art GMP manufacturing facilities operate under a rigorous quality and Environmental, Health, and Safety (EHS) system, ensuring compliance with global regulatory standards, including those of the United States, European Union, China, and Japan. As a one-stop solution provider, we support the entire drug development lifecycle—from early discovery and clinical trials to commercial-scale manufacturing. By adhering to stringent FDA and ICH CGMP guidelines, we deliver products of the highest quality standards and provide comprehensive regulatory assistance, including the preparation and submission of Drug Master Files (DMFs). With expertise in generic (ANDA) and New Chemical Entity (NCE) development, including NDA submissions, we ensure efficient and reliable pathways for regulatory approval, enabling seamless transitions from concept to commercialization.

Dispensary of Hope
The Dispensary of Hope is a charitable wholesale medication distributor located in Nashville, Tennessee serving America’s safety net of free and charitable clinics, community health centers and charitable pharmacies. Through innovative stewardship of the pharmaceutical supply-chain, the Dispensary of Hope collects and distributes millions of dollars of donated pharmaceuticals annually to these licensed healthcare organizations to dispense to low income, uninsured patients free of charge. Pharmacies and clinics utilize Dispensary of Hope medication to address community health concerns, as the cornerstone of avoidable hospital readmission programs and to reduce unnecessary emergency room use that often results from lack of access to essential medication. Staff and operations meet the highest medication distribution standards, from manufacturer to the dispensing site – as evidenced by industry accreditations and memberships (National Association of Boards of Pharmacy, MedSurplus Alliance, Association for Accessible Medicines and Healthcare Distribution Alliance) and strict adherence to the Drug Supply Chain Security Act. Learn more at www.dispensaryofhope.org.

DisposeRx
DisposeRx, based in Southern Pines, NC, makes it easy to safely dispose of unused medications at home. Our simple, effective solutions help prevent accidental poisonings, misuse, and overdose—protecting families and communities.By focusing on prevention and creating products anyone can use, we’re tackling the the prescription crisis head-on and raising the standard for medication safety. At DisposeRx, we believe protecting your health and the environment starts with responsible medication disposal. Together, we can help create safer, healthier communities by eradicating the misuse of unused prescription drugs.

Eirgen Pharma
Eirgen Pharma is a research-driven company that specializes in the development, manufacture and supply of a broad range of High Potency Oral Solid Dose (OSD) Human & Veterinary specialty products. Eirgen Pharma simplifies the journey from molecule to market through cutting-edge research, development and manufacture.With decades of combined industry-leading experience and 15 years of working as a unit, the Eirgen Pharma team has helped to develop and launch drugs across multiple markets. This includes high potency medicines for a variety of therapeutic areas such as cancer chemotherapy and veterinary drug formulation. At Eirgen Pharma’s centre of excellence, your project is in the safest of hands.

Lachman Consultant Services, Inc.
Through our long-standing mastery of technical and regulatory consultation services, Lachman Consultants serves all areas of FDA-related activities for the Pharmaceutical, Biotechnology, Biologics, Diagnostic, Device and Allied Health Industries. We serve a diverse base of loyal clients around the globe, from emerging-to-enterprise organizations across virtually any specialty of the life sciences. The associates of Lachman Consultants are proficient in the development, implementation and management of diversified projects involving scientific principles, technical aspects and regulatory requirements.

LifeScience Logistics
LSL is the premier leader of supply chain solutions, proudly focused on and purpose-built exclusively for the healthcare industry to support pharmaceutical and medical device manufacturers, government entities, and other healthcare organizations. Our goal is to advance public health by strengthening the supply chain and ensuring seamless end-to-end logistics for the manufacturing, distribution, and storage of critical healthcare products.

MAP International
MAP is a global health and relief organization on a mission to end the global health crisis and bring medicines to all people around the world.

Medical Packaging Inc., LLC
Medical Packaging Inc., LLC (MPI) is a leading global manufacturer of unit dose medication and pharmaceutical packaging and labeling systems, barcode labeling software, and MPI-certified consumable materials. MPI delivers superior oral solid and liquid cup unit dose packaging systems which are carefully designed to meet the needs of the pharma industry and healthcare sector. The FD-Pharma® system is an ideal liquid medication packaging solution, enabling customers in these markets to add FDA-compliant liquid cup packaging capabilities to their manufacturing operations at a low cost. Our Drug Master File (DMF) allows us to provide greater efficiency to partners with speed-to-market regulatory and technical support. MPI remains dedicated to meeting the evolving needs of biosimilars and generics, ensuring the safety and effectiveness of these medications through innovative packaging solutions.

MedPharm
Leading Topical and Transdermal Drug Development Founded in 1999 out of King’s College London, MedPharm has grown into a premier end-to-end contract development and manufacturing organization (CDMO) specializing in topical, transdermal, and transepithelial pharmaceutical products. With facilities in Guildford, UK, and Durham, NC, USA, we provide comprehensive services spanning formulation, analytical development, in vitro testing, clinical trial material supply, and commercial manufacturing. Renowned for our expertise in semi-solid and liquid formulations, MedPharm supports clients across more than 30 countries. Our proprietary technologies and innovative in vitro models expedite development timelines, reduce risk, and provide unparalleled insights into drug efficacy and delivery. From addressing complex delivery routes—such as dermal, nasal, and ocular—to shipping FDA-approved commercial products, MedPharm offers a seamless pathway from concept to market. With a commitment to quality and regulatory excellence, we’ve facilitated the development of over 80 commercial products and continue to push the boundaries of pharmaceutical science. MedPharm’s dedication to precision, innovation, and collaboration ensures your product’s success at every stage of development. For more information, visit medpharm.com.

Nutra-Med Packaging LLC
Nutra-Med Packaging LLC provides rapid packaging services for the Pharmaceutical, OTC, medical device, diagnostics, and dietary supplement industries for the US and ROW. While we continue to focus on solid oral blister packaging and bottling, we are also providing specialized kitting, cartoning, and serialization operations for a variety of dosage forms and devices including vials and PFS.

PharmaHub
PharmaHub® is a web based search portal which aggregates and simplifies cumbersome pharmaceutical data from the FDA OrangeBook, Medicare & Medicaid, VA FSS and the US Patent and Trade Office. For pharma due diligence it is a crucial time saver and delivers cross-referenced answers to your queries for multiple departments: Business Development, Regulatory, Legal and M&A.m.

Phlow Corp.
Phlow is a U.S.-based, Certified B Corporation™ leveraging advanced manufacturing processes to re-imagine the domestic production of key starting materials (KSM), active pharmaceutical ingredients (API), and finished drug products that are critical to U.S. healthcare. Focused on impact, Phlow partners with children’s hospitals, private industry, and the U.S. government to increase access to affordable, high-quality, life-changing medicines through advanced manufacturing processes that are fully integrated, comprehensive, and better for the environment. Utilizing its advanced R&D labs and best-in-class, automated API cGMP facilities ranging from kilo to metric ton scales, Phlow provides customized contract development and manufacturing services for small molecule APIs to pharmaceutical and biotech companies. Phlow measures its success by driving down costs and waste, improving quality and yield, and offering a more environmentally friendly approach to manufacturing medicines that lead to healthy and resilient communities. For more, visit www.phlow-usa.com.