Upcoming program exhibitors

Outsourced Pharma conferences form intimate and impactful leadership communities for sponsors and suppliers. It’s where pharma and biotechs engage directly in dialogue with contract service providers, leading to business opportunities on both sides.

Which CMOs have the capabilities of handling your production processes? Is there someone new to discover?

Exhibitors by Show Exhibitor Profiles

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Exhibitors by Show

San Diego 2017

Advinus Therapeutics
Albemarle
Alcami Corporation
Althea CMO
Ash Stevens
Avara Pharmaceutical Services
Avista Pharma Solutions
Berkshire Sterile Manufacturing
Cambrex Corporation
CordenPharma
DavosPharma
Dottikon ES America, Inc.
EAG Laboratories
Emergent Biosolutions
FAREVA
Masy BioServices
Metrics Contract Services
PCI Pharma Services
Pharmatech Associates
Quotient Clinical

Ricerca
Rondaxe
SMC, Ltd.
Sherpa Clinical Packaging
Siegfried USA, LLC
Triclinic Labs
Unither Manufacturing LLC
WuXi AppTec
Yourway Transport
Sponsors: TBA

 

View Floorplan

 

San Francisco 2017

Albemarle
Alcami Corporation
Almac
Althea CMO
Ash Stevens
Avara Pharmaceutical Services
Avista Pharma Solutions
B. Braun Medical OEM
Berkshire Sterile Manufacturing
BioDuro
Cambrex Corporation

CMC Biologics
Cytovance Biologics
Dottikon ES America, Inc.
Flamma S.p.A.
FAREVA
FUJIFILM Diosynth Biotechnologies
LI-COR Biosciences
Metrics Contract Services
PCI Pharma Services
PCI Synthesis

Pharmatech Associates
Quotient Clinical
Ricerca
Rondaxe
Sherpa Clinical Packaging
Siegfried USA, LLC
Therapure Biopharma
Triclinic Labs
Unither Manufacturing LLC
Yourway Transport
Sponsors: TBA

 

View Floorplan

 

Interested in exhibiting? Get in touch for details.

 

 

2017 Exhibitor Profiles

Advinus Therapeutics

Advinus Therapeutics

San Diego Booth 25

Advinus is GLP-certified, AAALAC-accredited and the first CRO in India which has been inspected by USFDA. We offer end-to-end cGMP and GLP capabilities for pre-clinical development of molecules, including process development, DMPK and Regulatory Toxicology for developing full CMC & Pharmtox packages toward an IND submission. We have submitted 50 complete IND packages and conducted over 60 carcinogenicity studies for global clients and have the experience of having conducted over 10,000 regulatory studies including acute to chronic, Juvenile, reproduction and carcinogenicity studies in RasH2 & p53 Transgenic mouse models. We also offer non-clinical Regulatory Toxicology packages targeted towards NDA submission.

Anjali Nanda , Marketing | +91-9916180482

 

21& 22 Phase II, Peenya Industrial Area | Bangalore 560058 India
Albemarle

Albemarle

San Diego Booth 28 | San Francisco Booth 21

Albemarle has been an industry leader in contract pharmaceutical, agrichemical, lubricant and specialty chemicals manufacturing for over 40 years. Our world-class facilities and advanced R&D capabilities enable our Fine Chemistry Services team to aid in every stage of product development ― from contract research through commercial-scale manufacturing. As a worldwide leading producer of lithium and bromine, Albemarle’s well-conceived back integration allows for near seamless access to important raw materials, as well as critical knowledge of unique chemistries. Albemarle implements cGMPs at our Active Pharmaceutical Ingredient manufacturing facility in South Haven, MI and offers ISO quality manufacturing services at Tyrone PA.

Julie Risdon, Global Business Manager | 269-639-0113

 

4350 Congress Street, Suite 700 | Charlotte, NC 28209

 

Alcami Corporation

Alcami Corporation

San Diego Booth 30 | San Francisco Booth 56

Alcami is a world-class supplier of comprehensive pharmaceutical development and manufacturing services. With seven sites across the globe, our combined capabilities include API development and manufacturing, solid state chemistry, formulation development, analytical development and testing services, clinical and commercial finished dosage form manufacturing (oral solid dose and parenteral), packaging, and stability services.

Lindsay Logan, Marketing Communications Specialist | 910-254-7175

 

2320 Scientific Park Drive | Wilmington, NC 28405

 

Almac Group

Almac Group

San Francisco Booth 80

Almac Group is an established, leading contract development and manufacturing organisation providing an extensive range of integrated services to over 600 pharmaceutical and biotech companies globally. Its Pharma Services Business Unit offers services including pharmaceutical product launch & distribution, commercial drug product manufacture, commercial packaging, serialisation and commercial storage & distribution. The privately owned, global organisation has grown organically over 45 years now employing in excess of 4,500 highly skilled personnel and has a strong reputation for innovation, quality and exceptional customer service. The Group is headquartered in Craigavon, Northern Ireland with additional operations based throughout Europe, US and Asia.

David Downey , VP Commercial Operations | +44 (0) 28 3836 3363

 

20 Seagoe Industrial Estate | Craigavon BT63 5QD United Kingdom

 

Althea CMO

Althea CMO

San Diego Booth 35 | San Francisco Booth 69

Althea is a fully integrated, contract development and manufacturing organization located in San Diego, CA providing clinical and commercial product development services. Althea offers cGMP drug product filling in both vials and syringes, and production of microbial-derived recombinant proteins and plasmid DNA. Althea also offers process development, analytical development, complex formulation, release testing, and stability testing services. Learn more at www.altheacmo.com.

Matt Codd, Director, Business Development | 858-210-0730

 

11040 Roselle Street | San Diego, CA 92121

 

Ash Stevens

Ash Stevens, LLC

San Diego Booth 08 | San Francisco Booth 42

Ash Stevens, LLC is a division of Piramal Pharma Solutions offering comprehensive contract drug substance development and active pharmaceutical ingredient (API) manufacturing services. With more than 50 years of experience, Ash Stevens has 14 FDA manufacturing approvals (NCEs) for small molecule APIs, including multiple fast-track approvals for oncology drugs. Ash Stevens is also a long-time provider of potent compound manufacturing (HPAPI) services with an exemplary safety record and global regulatory inspection history. Services offered by Ash Stevens include process development, HPAPI manufacturing, cGMP manufacturing, preparation of documents for regulatory submissions (IND, NDA, DMF, CTD), and comprehensive analytical and regulatory support.

James Hamby , Vice President, Business Development | 734-776-1476

 

18655 Krause Street | Riverview, MI 48193

 

Avara Pharmaceutical Services

Avara Pharmaceutical Services

San Diego Booth 33 | San Francisco Booth 22

Avara Pharmaceutical Services delivers world class contract manufacturing and technical services to the biopharmaceutical market. Our broad experience with supply chain, commercialization, product launch and product transfer allows us to sustain exemplary levels of product quality and regulatory compliance. We are known to exceed customer service level expectations and we pride ourselves with our on time and in full record, at a fair price. Our extensive experience of supply ranges from the U.S. to international markets. Our Manufacturing and Packaging capabilities are equipped to work with oral solid dosage (tablets and capsules) and includes a high-containment module.

William L. Pasek, Executive Vice President, Chief Commercial Officer | 203-655-1333

 

101 Merritt 7 | Norwalk, CT 06851

 

Avista Pharma Solutions

Avista Pharma Solutions

San Diego Booth 52 | San Francisco Booth 12

Avista Pharma Solutions, Inc. is a leading contract testing, development and manufacturing organization (CDMO). Encompassing over 200,000 square feet of laboratory and manufacturing space across three Centers of Excellence (Agawam, MA – Durham, NC – Longmont, CO), Avista Pharma provides pharmaceutical, animal health and medical device clients with a broad suite of scientifically differentiated services and pharma solutions. Services range from early stage discovery, API and Drug Product development and cGMP manufacturing to stand-alone analytical and microbiology testing support.

Tim Compton , VP, Business Development | 910-622-0529

 

3501 Tricenter Boulevard, Suite C | Durham, NC 27713

 

B. Braun Medical OEM

B. Braun Medical OEM

San Francisco Booth 66

B. Braun OEM Division designs and manufactures a variety of standard and custom products for the pharmaceutical, biotech and medical device markets, including valves, reconstitution and transfer devices, fluid delivery systems, custom kits, and solutions. B. Braun takes customers’ designs from the earliest stages through prototyping, assembly, packaging and sterilization.

Philip Milia , OEM Account Manager | 610-691-6785

 

824 12th Avenue | Bethlehem, PA 18018

 

Berkshire Sterile Manufacturing

Berkshire Sterile Manufacturing

San Diego Booth 42 | San Francisco Booth 30

Berkshire Sterile Manufacturing (BSM) has two main objectives: 1. To surround their clients’ products with the highest level of sterility assurance; 2. To supply a flexible and customer centric environment for their clients. BSM has the most flexible and high performance technologies for filling into syringes, vials, and cartridges within isolated environments. BSM has support equipment and facilities, such as analytical lab, micro lab, walk-in controlled temperature storage areas, stability chambers, etc… to support your drug or sterile device production. This is coupled with a robust quality system to ensure the highest level of sterility assurance and quality achievable.

Andrea Wagner, SVP Business Development | 413-243-0330 x102

 

480 Pleasant Street | Lee, MA 01238

 

BioDuro

BioDuro

San Francisco Booth 37

BioDuro is a biopharmaceutical development and manufacturing organization specializing in drug discovery, dosage form development and GMP manufacturing, and we provide a variety of solutions that can help our customers in efficient drug delivery. Our services include end-to-end solutions from drug discovery to drug product development and GMP manufacturing. From simple API in a capsule to high-performance pharmaceutical formulations, such as hot-melt extrusion and spray drying, BioDuro has extensive drug development experience bringing client compounds from early phase development to commercial launch.

Eric Lee, Marketing Manager | 858-529-6600

 

11011 Torreyana Road | San Diego, CA 92121
Cambrex Corporation

Cambrex Corporation

San Diego Booth 17 | San Francisco Booth 17

Cambrex is an innovative life sciences company that provides pharmaceutical products, expertise and technologies that accelerate small molecule therapeutics into markets across the world. With over 35 years of active pharmaceutical ingredient development (API) and manufacturing expertise, a team of more than 1,200 experts and a strong presence in the USA and Europe, Cambrex is tried and trusted across branded and generic API markets. Cambrex offers an end-to-end partnership for the research, development and manufacture of small molecule APIs at every stage of the lifecycle. Its capabilities include classical and advanced chemistry, enzymatic biotransformations, high potency APIs, high energy chemical synthesis and controlled substances.

George Rothermel, Director, Sales and Business Development | 980-254-1121

 

One Meadowlands Plaza | East Rutherford, NJ 07073
CMC Biologics

CMC Biologics

San Francisco Booth 35

CMC Biologics, a global Contract Development and Manufacturing Organization (CMO), has three biomanufacturing facilities in Europe and USA. We are an industry leading CMO who is consistently recognized in reliability, technical excellence, and quality – Right and On Time. The Company provides a comprehensive range of clinical and commercial cGMP biologics development and manufacturing services, from DNA to API. The Company’s team and approach are tailored to the client’s needs, whether turnkey manufacturing or stand-alone analytical, formulation and stability services. CMC Biologics also offers license to CHEF1™, a proprietary CHO cell line expression technology platform. Visit cmcbio.com to learn more.

Benjamin Gorenberg, Marketing Manager | 425-489-5042

 

22021 20th Avenue SE | Bothell, WA 98021

 

CordenPharma

CordenPharma

San Diego Booth 22

CordenPharma is your full-service partner in the Contract Development & Manufacturing (CDMO) of APIs, Drug Products and associated Packaging Services. Through a network of fully-inspected cGMP facilities across Europe and the US organized under five technology platforms – Peptides, Oligonucleotides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, Antibiotics - CordenPharma experts translate complex ideas at any stage of development into high-value products.

Celia Alexander , Associate Director, Sales & Key Account Management | 720-683-9996

 

2075 55th Street | Boulder, CO 80301

 

Cytovance Biologics

Cytovance Biologics

San Francisco Booth 11

Cytovance® Biologics is a contract development manufacturing company specializing in the cGMP production of therapeutic proteins and antibodies from mammalian cell culture, microbial fermentation, transgenic processes, and small scale “flex suite” programs. In addition, Cytovance offers process development services, cell line development, purification development, stability testing, and regulatory support services – all from its Oklahoma City state-of-the-art facilities. Cytovance partners with clients to provide integral pathways in converting novel protein discoveries into lifesaving therapies.

Cheryl Soerensen (Tuck), Marketing Communication Manager | 405-319-8309

 

800 Research Parkway, Suite 200 | Oklahoma City, OK 73104

 

DavosPharma

DavosPharma

San Diego Booth TBD

Profile coming soon.

 

Address TBA
Dottikon ES America, Inc.

Dottikon ES America, Inc.

San Diego Booth 61 | San Francisco Booth 67

DOTTIKON ES manufactures high-quality performance chemicals, intermediates and exclusive active pharmaceutical ingredients (APIs) for the world's leading chemical and pharmaceutical industry. The company with its production site in Dottikon (Aargau, Switzerland) is specialized in hazardous reactions and is positioning itself as strategic development and manufacturing partner. Its safety culture created over the last 100 years guides innovative use of hazardous reactions, low-temperature and high-pressure chemistry, as well as continuous processing. This shortens conventional chemical synthesis routes, increases yields, selectivities and purities, and reduces waste. The versatile technology and equipment portfolio is used to design, develop and optimize chemical processes, and scale up from kilograms to multi-tons. DOTTIKON ES' one-site strategy allows reduced decision and communication pathways. This ensures rapid and efficient project development as well as clear and transparent communication with customers.

Sean Bradley, Head of Business Development US | 001-862-251-1352

 

Hembrunnstrasse 17 5605 | Dottikon, Switzerland

 

EAG Laboratories

EAG Laboratories

San Diego Booth TBD

EAG Laboratories (formerly ABC Laboratories) is an analytically focused CRO with experience in method development, program design and complex study execution, EAG Laboratories offers the pharmaceutical industry a true development CRO. We deliver comprehensive CMC analytical support including multi-disciplinary, multi-technique analytical method development and validation, complete stability program management and in-depth extractables and leachables expertise—plus in-house custom synthesis and cGMP radiolabeling services. A global scientific services company, EAG also offers specialized materials testing to support supply chain and packaging initiatives, and the full range of studies required for pharmaceutical environmental risk assessments. How do you make better development decisions faster?

Cindy Gentile, Sr. Marketing Analyst | 408-530-3776

 

4780 Discovery Drive | Columbia, MO 65201

 

Emergent BioSolutions

Emergent BioSolutions

San Diego Booth 34

Emergent BioSolutions (acquirer of Cangene bioPharma) provides contract manufacturing services for both bulk drug substances and finished drug products. Emergent’s state-of-the-art single-use BDS facility enables turnkey upstream and downstream support for microbial, mammalian and viral cell lines. Emergent’s Fill/Finish service offering includes vials and syringes, for both liquid and lyophilized products (including lyo cycle development). Emergent’s manufacturing facilities (located in Baltimore, MD) currently produce 20 commercial products and supported over 200 clinical drug products.

Patrick DePalma, Director, Business Development | 410-736-0631

 

1111 South Paca Street | Baltimore, MD 21230

 

Flamma S.p.A.

Flamma S.p. A.

San Francisco Booth 20

Profile coming soon.

 

Address TBA

 

FAREVA

FAREVA

San Diego Booth 17 | San Francisco Booth 31

Fareva ranks in the top five largest Contract Manufacturing Organizations in the world by revenue. The company generated revenue of €1.3 billion in 2014. The company has more than 9,500 employees located at 35 sites in 12 countries. Our API division focuses on process chemistry, analytical development and drug substance manufacturing for both clinical trials and commercial production. Fareva has a broad range of capacity with programs ranging from 1kg to 50 metric tons. The company has niche technology for aseptic crystallization and micronization, high potent APIs, cytotoxics and steroids. Fareva is the first and only company in the world to receive SafeBridge Certification to handle both high potent drug substance and drug product at the same facility. Fareva also has formulation and drug product capability including: tablets, capsules, sprays/aerosols, sterile solutions/suspensions, liquid forms/gels, powder filling, suppositories, blow fill seal, and high potent pharmaceuticals. Fareva’s facilities are FDA inspected and the company has an excellent track record and experience with regulatory agencies worldwide.

George Hlass , Senior Director, API Business Development, North America | 919-768-6858

 

24 West 57th Street | New York, NY 10019

 

FUJIFILM Diosynth Biotechnologies

FUJIFILM Diosynth Biotechnologies

San Francisco Booth 28

FUJIFILM Diosynth Biotechnologies is a world leading cGMP Contract Development and Manufacturing Organization supporting our partners in the biopharmaceutical industry in the development and production of their therapeutic candidates. As a global organization we operate as a network with locations in Research Triangle Park, North Carolina, USA; College Station, Texas, USA and Billingham, United Kingdom. As a partner to our customers, we bring extensive process and analytical development and cGMP manufacturing experience to meet your needs at every stage of the product lifecycle, from efficient protein expression, process design and cGMP manufacture, through to process validation, commercial production, and post approval product lifecycle management.

Anitra Johnson, Sr. Marketing Specialist | 919-337-4409

 

101 J. Morris Commons Lane | Morrisville, NC 27560
LI-COR Biosciences

LI-COR Biosciences

San Francisco Booth 48

LI-COR Biosciences offers custom services to assist scientists with unique needs or requirements that off the shelf products can’t meet. This includes labeling proteins, antibodies, peptides and small molecules, and cGMP production. We are the leading innovator of infrared dye applications and technology for molecular imaging. With more than 45 years of experience in research from measuring global climate change to novel protein and in vivo imaging applications, LI-COR provides innovative instruments, software, reagents, and integrated systems for researchers worldwide. LI-COR is an ISO 9001:2008 certified company, and its mission is Impacting Lives Through Science.

 

4647 Superior Street | Lincoln, NE 68504
Masy BioServices

Masy BioServices

San Diego Booth TBD

Masy BioServices’ integrated suite of metrology, qualification, and offsite cGMP biorepository services helps life science companies improve the quality and accuracy the product development chain — from ensuring the accuracy of primary standards and measurement instrumentation, through qualifying laboratory equipment and environmental chambers, to secure storage of samples and finished products.

Branden Morris , Director of Marketing | 978-433-6279

 

10 Lomar Park Drive | Pepperell, MA 01463

 

Metrics Contract Services

Metrics Contract Services

San Diego Booth TBD | San Francisco Booth TBD

Metrics Contract Services is a full-service pharmaceutical development and manufacturing organization serving clients worldwide. We deliver proven scientific and operational excellence for solid oral dosage forms. Our expertise includes quality formulation development; first-time-in-man formulations; Phase I-III clinical trial materials manufacturing; and analytical method development and validation services leading to commercial scale manufacturing. Our technical capabilities include highly potent, cytotoxic and unstable compounds; DEA Schedule II-V controlled substances; and products with poor bioavailability, for which we offer advanced delivery methods. Located in Greenville, N.C., Metrics Contract Services is a proud member of the Mayne Pharma family. Learn more at http://www.metricsinc.com.

John Ross, Executive Vice President | 252-317-3903

 

1240 Sugg Parkway | Greenville, NC 27834

 

PCI Pharma Services

PCI Pharma Services

San Diego Booth 29 | San Francisco Booth 29

PCI Pharma Services is an integrated full service provider, a proven and trusted partner to leading companies in the global healthcare industry. We offer unparalleled expertise and experience in taking compounds from the earliest stages of development through to successful commercialization, delivering speed-to-market and commercial success for our customers. We have combined the expertise of Penn Pharma, Biotec Services International, AndersonBrecon, and Packaging Coordinators to create PCI, an integrated pharmaceuticals provider positioned to support your drug needs from molecule to market. We invite you to learn more about how partnering with PCI can ensure the success of your product.

Justin Schroeder , Exec. Director, Marketing, Bus. Dev., & Design Services | 815-484-8973

 

3001 Red Lion Road | Philadelphia, PA 19114

 

PCI Synthesis

PCI Synthesis

San Francisco Booth 39

PCI Synthesis is a Pharmaceutical Development CMO (Contract Manufacturing Organization) based in Newburyport, MA and is the largest small molecule drug substance manufacturer in the New England area. PCI is also a commercial manufacturer of new chemical entities (NCEs), generic active pharmaceutical ingredients (APIs), and other specialty chemical products for the medical device industry. As a contract manufacturing organization (CMO), PCI provides emerging and mid-sized pharmaceutical companies access to the expertise needed to develop and manufacture complex small molecules. To learn more about PCI Synthesis, its proprietary NCE development activities and process R&D capabilities please visit www.pcisynthesis.com.

Ed Price , President | 978-463-4888

 

9 Opportunity Way | Newburyport, MA 01950

 

Pharmatech Associates

Pharmatech Associates

San Diego Booth 27| San Francisco Booth 24

Pharmatech Associates provides consulting and services to the regulated life science industry. Pharmatech’s services cover four spheres of technical expertise that are necessary throughout the complete product development lifecycle: Product and Process Development, Compliance, Regulatory, and Validation. It is this interconnected framework of services which denotes The Pharmatech EcosystemTM. Pharmatech advises clients that range in size from startups to large multi-national corporations on projects in Asia, Europe and North America from its headquarters in the San Francisco Bay Area.

Pete Rafa, Associate Director, Project Design & Start Up | 510-732-0177

 

22320 Foothill Boulevard, #330 | Hayward, CA 94541

 

Quotient Clinical

Quotient Clinical

San Diego Booth 39 | San Francisco Booth 10

Quotient Clinical is a drug development service provider, delivering formulation development, GMP manufacturing and clinical pharmacology. By integrating make (CDMO) and test (CRO) services, our unique and innovative Translational Pharmaceutics® platform is proven to significantly accelerate drug development timelines and reduce costs. We employ over 600 staff and operate from state-of-the-art manufacturing and clinical facilities in the UK and USA, including three clinical pharmacology centres housing 400 beds. We can support our clients by working under FDA or MHRA guidelines and offer a full range of support services, from study set-up right through to data analysis and reporting.

Matthew Paterson , Vice President, Business Development (North America) | 410-926-9191

 

Mere Way Ruddington | Nottingham NG11 6JS UK

 

Ricerca

Ricerca

San Diego Booth 40 | San Francisco Booth 32

Ricerca is a contract research and manufacturing organization offering first-class analytical chemistry, synthetic chemistry, engineering, and API manufacturing services throughout all phases of drug development. From preclinical development to commercial manufacturing, Ricerca offers flexible access to a broad spectrum of development and manufacturing expertise. Our highly experienced scientific team has a proven history of achievement with complex chemistry challenges providing a complete solution for your small molecule chemical development needs. For more than 25 years, Ricerca has a record of on-time delivery and quality, providing comprehensive support and problem solving for successful development, scale-up, and process-optimized manufacture of pharmaceutical ingredients.

Michael Contenza , Senior Director/Business Manager -- Chemical Development | 440-357-3161

 

7528 Auburn Road | Concord, OH 44077

 

Rondaxe

Rondaxe

San Diego Booth TBD | San Francisco Booth TBD

Rondaxe is a full-service pharmaceutical CMC consultancy led by an experienced team of industry executives and 50+ senior advisors with extensive industry experience. Since our founding in 2003, we have helped clients around the globe solve manufacturing problems, prepare CMC sections for submission, raise money, and form partnerships. Rondaxe’s experts are our most important asset. The combined knowledge and experience of our project teams deliver exceptional results for our clients. Building from our core expertise in CMC, Rondaxe’s capabilities have expanded to include a unique suite of software. We are constantly improving to meet our clients’ growing needs.

Joel R. Lirot, Vice President Business Development | 315-469-2800 x303

 

6443 Ridings Road, Suite 125 | Syracuse, NY 13206

 

SMC, Ltd.

SMC, Ltd.

San Diego Booth TBD

Profile coming soon.

 

Address TBA
Sherpa Clinical Packaging

Sherpa Clinical Packaging

San Diego Booth 41 | San Francisco Booth 47

Sherpa is a San Diego based leading provider of Clinical Trial Material management services, including packaging, labeling, distribution and returns, for pharmaceutical, biotechnology, and medical device companies of all sizes. We offer innovative and cost effective solutions while delivering the highest quality service and reliability. Sherpa offers the flexibility and speed to help clients meet challenging schedules, while delivering services of the highest quality. Sherpa specializes in cold-chain management, and can process, store and distribute materials at tightly controlled temperatures.

Mark Paiz, President | 858-997-1491

 

6166 Nancy Ridge Drive | San Diego, CA 92121

 

Siegfried USA, LLC

Siegfried USA, LLC

San Diego Booth TBD | San Francisco Booth TBD

Profile coming soon.

 

Address TBA
Therapure Biopharma

Therapure Biopharma

San Francisco Booth 65

Profile coming soon.

 

Address TBA

 

Triclinic Labs

Triclinic Labs

San Diego Booth 47 | San Francisco Booth 57

Triclinic Labs provides leading solid-state polymorph, pharmaceutical salt, cocrystal, and amorphous material screening, selection, and development services. We offer extensive analytical chemistry services to support routine sample analyses, problem solving, and method development. Triclinic Labs provides proven chemistry-based scientific expertise, consulting and experimental services. We support patent prosecution and litigation. Our experts have extensive experience in more than 100 matters worldwide. Triclinic experts will support your team with tested experimental approaches and analyses. Our goal: clear authoritative opinions, timely experimental results, and expert testimony. Visit www.TriclinicLabs.com or contact us today for a free consultation or quotation.

Shawn Comella , CEO | 765-588-5624

 

2660 Schuyler Avenue, Suite A | Lafayette, IN 47905

 

Unither Pharmaceuticals

Unither Pharmaceuticals

San Diego Booth 46 | San Francisco Booth 27

Unither Pharmaceuticals’ affordable and convenient unit dose formats can improve medication adherence and help translate clinical trial success into the marketplace. Patients appreciate the benefits of our technologies: accurate single-dose dispensing without a measuring device, portability for use, elimination of preservatives, and improved hygiene through single use. Since inception in 1993, we have grown to become a world leader in the development and manufacturing of unit dose forms: Blow-Fill-Seal (BFS) and Unistick™. Expansion of our Rochester, NY, USA, facility and acquisition of our newest facility in Barretos, Brazil, further establish Unither as a global partner.

Anthony Reda, Executive Director Business Development | 585-274-5447

 

755 Jefferson Road | Rochester, NY 14623

 

WuXi AppTec

WuXi AppTec

San Diego Booth 54

WuXi AppTec is an innovation-driven, leading global pharmaceutical, biopharmaceutical, and medical device outsourcing company with US and China operations helping customers shorten R&D timelines and lower R&D costs through cost-effective efficient solutions. WuXi AppTec subsidiary STA Pharmaceutical is a trusted global partner for pharmaceutical development & manufacturing. End-to-end drug substance services including API development and manufacturing, chemical synthesis route selection, process development and optimization, scale-up process research and is capable of producing intermediates and APIs from kg to metric ton scale. Drug product services include developablity & formulation research, formulation development & optimization, phase I-III clinical supplies including cGMP manufacturing.

Yu Lu, Executive Director, Corporate Development and Communications | 609-516-0664

 

6114 Nancy Ridge Drive | San Diego, CA 92121

 

Yourway Transport

Yourway Transport

San Diego Booth 38 | San Francisco Booth 45

Profile coming soon.

 

Address TBA