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

Boston 2017 

AMRI
Adesis, Inc.
Albemarle
Alcami Corporation
Almac
Althea CMO
Ascendia Pharmaceuticals
Ash Stevens
Avara Pharmaceutical Services
Avista Pharma Solutions
B. Braun Medical OEM
Berkshire Sterile Manufacturing
BioDuro
Cambrex Corporation
Cardinal Health
CMC Biologics
CordenPharma



Corning
Cytovance Biologics
Dottikon ES America, Inc.
Emergent Biosolutions
Eurogentec S.A.
FAREVA
FUJIFILM Diosynth Biotechnologies
Genovior Biotech Corp.
LSNE
Masy BioServices
Metrics Contract Services
Paragon Bioservices
Patheon
PCI Pharma Services
PCI Synthesis
Pharmatech Associates


PharmAssist Analytical Laboratory
Quotient Clinical
Ricerca
Richter-Helm BioLogics
SGS Life Sciences
SafeBridge Consultants, Inc.
Sherpa Clinical Packaging
Solid Form Solutions
SynConnection
Tepnel Pharma Services
Triclinic Labs
Unither Pharmaceuticals
UPM Pharmaceuticals
Vetter
Wacker Biotech GmbH
WuXi AppTec
Sponsors: Solvias | Fermion OY, Orion Group | LuinaBio Pty Ltd. | Rondaxe

 

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San Diego 2017

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

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

 

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San Francisco 2017

Albemarle
Alcami Corporation
Almac
Ash Stevens
Althea CMO
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
Sherpa Clinical Packaging
Siegfried USA, LLC
Therapure Biopharma
Triclinic Labs
Unither Manufacturing LLC
Yourway Transport
Sponsors: TBA

 

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Interested in exhibiting? Get in touch for details.

 

 

2017 Exhibitor Profiles

AMRI

AMRI

Boston Booth 105 

AMRI is a global contract research and manufacturing organization that has been working with the Life Sciences industry to improve patient outcomes and quality of life for over twenty-five years. AMRI specializes in diverse chemistry, biology and pharmacology, and complex API and drug product manufacturing, from initiation to commercialization.

Melissa Allard, Client Services | 518-512-2542

 

26 Corporate Circle | Albany, NY 12212

 

Adesis, Inc.

Adesis, Inc.

Boston Booth 221

Adesis, Inc. is a US-only operated non cGMP chemistry CRO. We specialize in small molecule syntheses involving heterocycle chemistry, stable isotopes, reference standards and metabolite syntheses in mg to multi kg scale. Adesis has scientific depth with staffing versatility with over 50 chemists (80% Ph.D) split 50/50 between discovery chemistry and process/scale-up chemistry. Our versatile 25,000 sq ft facility is designed to be flexible to accommodate our clients needs. We have 25 years of proven performance with a 99% project success rate supporting clients in three areas: early stage research, scale up and development, and specialty manufacturing.

Paul Defina , Director, Business Development | 302-358-8837

 

27 McCullough Drive | New Castle, Delaware 19720

 

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

Boston Booth 213 | 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

Boston Booth 219 | 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

Boston Booth 106 | San Francisco Booth 80

Almac provide scalable development and manufacturing solutions, supporting all phases of clinical trials and ultimately commercialisation, from formulation to finished product. Specialising in the manufacture and primary packaging of solid oral dosage forms, our range of state-of-the-art equipment can meet your processing needs. With UK and US commercial packaging operations, we provide customised quality driven packaging solutions supporting both high-volume marketed products and niche/orphan drug launches. Providing the full service offering from development to commercialisation, we work with our clients to develop a strategic partnership, ensuring a smooth progression along the product lifecycle, mitigating risk, cost and shortening supply chains.

George Thibeault, Director, Business Development | 610-666-9500

 

2661 Audubon Road | Audubon, PA 19403

 

Althea CMO

Althea CMO

Boston Booth 108 | 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

 

Ascendia Pharmaceuticals

Ascendia Pharmaceuticals

Boston Booth 214

Profile coming soon.

 

Address TBA

 

Ash Stevens

Ash Stevens, LLC

Boston Booth 102 | 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

Boston Booth 217 | 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.

 

101 Merritt 7 | Norwalk, CT 06851

 

Avista Pharma Solutions

Avista Pharma Solutions

Boston Booth 103 | 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 Blvd, Suite C | Durham, NC 27713

 

B. Braun Medical OEM

B. Braun Medical OEM

Boston Booth 220 | 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

Boston Booth 207 | San Diego Booth 42 | San Francisco Booth 30

Profile coming soon.

 

Address TBA

 

BioDuro

BioDuro

Boston Booth 304 | 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 Rd | San Diego, CA 92121
Cambrex Corporation

Cambrex Corporation

Boston Booth 311 | 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
Cardinal Health

Cardinal Health

Boston Booth 301

Cardinal Health Regulatory Sciences provides scientific and regulatory consulting services to pharmaceutical, biotechnology and medical device companies to help them get their products to market quickly. For 40 years, we have provided services to companies around the world and have supported more than 100 product approvals. Our regulatory and product development strategies are designed to reduce the risk of failure and increase financial returns on your research investments. We provide efficient scientific and regulatory consulting services throughout the full product lifecycle to help ensure the continued success of your product post-approval.

Heather Reimer, Director, Business Development | 617-444-8768

 

245 First Street, Suite 1800 | Cambridge, MA 02142
CMC Biologics

CMC Biologics

Boston Booth 115 | 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

Boston Booth121 | 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

 

Corning

Corning

Boston Booth 205

Corning is a world-leading innovator in materials science. For over 165 years, we have applied our unparalleled expertise in glass science and precision process technologies to solve tough industry challenges and transform lives. Our innovations enhance quality and drive efficiencies in every industry that we serve. Learn more about Corning's solutions and services for the pharmaceutical industry.

Brendan Mosher , Sr. Business Development Manager | 607-974-4108

 

One Riverfront Plaza | Corning, NY 14831

 

Cytovance Biologics

Cytovance Biologics

Boston Booth 104 | 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.

Boston Booth 218 | 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

 

Dottikon Exclusive Synthesis AG Hembrunnstrasse 17 5605 | Dottikon, Switzerland

 

Emergent BioSolutions Inc.

Emergent BioSolutions Inc.

Boston Booth 201 | 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

 

Eurogentec S.A.

Eurogentec S.A.

Boston Booth 119

Eurogentec, part of Kaneka Corporation, is a leading supplier of specialty products and custom services. Through its three inter-related business units (Life Science Research, Diagnostic services and GMP BioManufacturing), the company provides high quality products to scientists involved in the life science, biotechnology, diagnostic and pharmaceutical markets. Eurogentec is ISO 9001, ISO 13485 certified, cGMP accredited by the Belgian Ministry of Health and approved by the US FDA for the manufacturing of a commercial biologic.

Alisson Pontus , Marketing Operations Executive | +32 372 74 00

 

Liege Science Park Rue Bois Saint Jean 5 4102 | Seraing Belgium
Flamma S.p.A.

Flamma S.p. A.

San Francisco Booth 20

Profile coming soon.

 

Address TBA

 

FAREVA

FAREVA

Boston Booth 200 | 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 | NY, NY 10019

 

FUJIFILM Diosynth Biotechnologies

FUJIFILM Diosynth Biotechnologies

Boston Booth 303 |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
Genovior Biotech Corp.

Genovior Biotech Corp.

Boston Booth 308

Genovior Biotech Corp., a vertically integrated contract development and manufacture company, providing following services: (a) process development of peptide or protein biologics from microbial or human recombinant fermentation processes (b) formulation development of injectables (c) manufacturing capacities of biologics, lyophilized injectables, and prefilled syringes/cartridges for clinical or commercial uses (d) process development of chemical API (e) formulation development and manufacturing capacities of oncology drugs (dedicated facility) Learn more at http://www.genovior.com.tw/

Emily Yeh, Associate Manager | +886 37 580280

 

4F., No. 50-8, Keyan Rd., Zhunan Township, Miaoli County 35053, Taiwan (R.O.C.)

 

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
LSNE

LSNE

Boston Booth 100

LSNE Contract Manufacturing is a CMO with a proven regulatory history specializing in a wide range of services including process development, fill/finish and lyophilization. LSNE has been providing cGMP services to the pharmaceutical, biotechnology and medical device industries since 1997. Through the thoughtful integration of three processing facilities, qualified staffing and an extensive manufacturing history, LSNE is strategically positioned to provide uninterrupted material for clinical through commercial use. LSNE’s experienced development, operations, quality and project management teams evaluate project objectives and recommend an optimal path forward to achieve easier regulatory submissions and a faster time to market.

Christine Palus, VP of Sales & Marketing | 603-668-5763

 

23 Commerce Drive | Bedford, NH 03110

 

Masy BioServices

Masy BioServices

Boston Booth 117

Profile coming soon.

 

Address TBA

 

Metrics Contract Services

Metrics Contract Services

Boston Booth 114

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

 

Paragon Bioservices

Paragon Bioservicese

Boston Booth 204

Paragon is an established Contract Development and Manufacturing Organization (CDMO), whose core business for over 26 years has been providing preclinical analytical development, process development and manufacturing services for a wide range of biopharmaceuticals. Paragon focuses on preclinical development and Phase I/II GMP manufacturing of all biologics including gene therapy products (recombinant viral vectors, rAAV), vaccines (whole cell, live virus, virus-like particles (VLPs), antigen-based, and conjugated), bacteriophage, and recombinant proteins. Paragon provides a turnkey, integrated set of services that can support early drug discovery through clinical manufacturing.

Emily Earll , Marketing Specialist | 410-975-4056

 

801 West Baltimore St. | Suite 302 Baltimore, MD 21201

 

Patheon

Patheon

Boston Booth 300

Patheon is a leading global provider of pharmaceutical development and manufacturing services. With approximately 8,700 employees worldwide, Patheon provides a comprehensive, integrated and highly customizable set of solutions to help clients of all sizes satisfy complex development and manufacturing needs at any stage of the pharmaceutical development cycle. A Healthier World. Delivered.

Victorri Taylor, Marketing Coordinator | 919-237-5617

 

4815 Emperor Blvd | Durham, NC 27703

 

PCI Pharma Services

PCI Pharma Services

Boston Booth 101 | 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., and Design Svcs | 815-484-8973

 

3001 Red Lion Road, Philadelphia, PA 19114

 

PCI Synthesis

PCI Synthesis

Boston Booth 116 | 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

 

PharmAssist Analytical Laboratory

PharmAssist Analytical Laboratory

Boston Booth 302

PharmAssist is a scientifically driven, high quality analytical laboratory that operates in full compliance with cGMPs and keeps abreast of developments in drug product regulatory requirements and analytical test method technology. Since 1989, PharmAssist has been providing superior analytical solutions to our customers in a cost-effective, timely manner.

Jeffrey Evans, CEO | 607-859-2702

 

3392 State Highway 8 PO Box 219 | South New Berlin, NY 13843
Pharmatech Associates

Pharmatech Associates

Boston Booth 118 | 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 Blvd. #330 | Hayward, CA 94541

 

Quotient Clinical

Quotient Clinical

Boston Booth 206 | 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

Boston Booth 209 | 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, Ohio 44077

 

Richter-Helm BioLogics

Richter-Helm BioLogics

Boston Booth 113

Richter-Helm BioLogics is a Germany-based contract development and manufacturing company specialized in products derived from bacteria and yeasts, with a 25-year track record. Clients worldwide have benefited from our commitment to good manufacturing practice and total transparency. Our work focuses on recombinant proteins, plasmid DNA, antibody fragments, and vaccines. Our team supports you with process development, supply of products for clinical trials, commercial production, in-house QC testing, and QP release. We operate two GMP-compliant production plants with bioreactor capacities of up to 1500 liters. Our quality standards have been verified by major regulatory bodies including EMA, FDA, ANVISA, and MFDS.

+49 (0)40 / 55 290 - 436

Dr. Antje Weingarth, Marketing & Sales | +49 (0)40 / 55 290 - 436

 

Suhrenkamp 59, 22335 Hamburg, Germany

 

SGS Life Sciences

SGS Life Sciences

Boston Booth 107

SGS Life Sciences is a leading contract service organization providing analytical development, biologics characterization, biosafety and quality control testing. With the largest network of 21 laboratories in 11 countries, services include: analytical chemistry, microbiology, stability studies, bioanalysis, extractables/leachables, virology and protein analysis.

Jessica Martin, Marketing & Sales Operations Manager | 847-821-8900

 

75 Passaic Avenue | Fairfield, NJ 07004

 

SMC, Ltd.

SMC, Ltd.

San Diego Booth TBD

Profile coming soon.

 

Address TBA
SafeBridge Consultants, Inc.

SafeBridge Consultants, Inc.

Boston Booth 203

SafeBridge Consultants, Inc. (“SafeBridge”) is the premier resource for high-level safety, health and environmental support to the pharmaceutical and biotechnology industry. SafeBridge is comprised of industry leaders in toxicology, analytical chemistry and industrial hygiene. Since 1998, SafeBridge has developed the “brand name” in the pharmaceutical industry as a leader in the field of advanced worker protection programs for potent API and product handling. SafeBridge has locations in Mountain View, California, New York City and Liverpool, England.

Catherine Connor , Business Development Assistant | 212- 727-0717 x217

 

330 7th Avenue, Suite 1101 | New York, NY 10001

 

Sherpa Clinical Packaging

Sherpa Clinical Packaging

Boston Booth 212 | 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
Solid Form Solutions

Solid Form Solutions

Boston Booth 216

SFS provides the pharmaceutical industry with integrated chemical and analytical development services. Our capabilities include: Salt/Polymorph/Co-Crystal Screening, Crystallization Screening & Process Development, Peptide Crystallization/Crystallization Scale-up, Particle Engineering & Size Control, Chiral Resolution/Single Crystal Analysis, HPLC Method Development & Validation, Stability Studies, Physical Properties and Developability Assessment, cGMP Release Testing, and Integrated Project Teams. Our services can either be used separately to solve specific problems, or in parallel to support a larger drug development campaign.

Julie Scott, Business Development Director | +441314408000

 

The Fleming Building Edinburgh Technopole, Milton Bridge | Nr. Penicuik, EH26 OBE, Scotland

 

SynConnection

SynConnection

Boston Booth 109

SynConnection offers world class Process R&D and cGMP manufacturing capabilities combining the assets of Syncom, ChemConnection and Austin Chemical. The development of novel active pharmaceutical ingredients demands a broad range of specialized technologies that should be combined to enable the shortest development time to clinicals. The SynConnection companies, building upon decades of pharmaceutical development history provide optimal chemical contract development services for small and mid-sized pharma and biotech companies. SynConnection offers specialized IND/IMPD enabling technologies including chiral resolution and process development, GMP manufacturing of highly potent materials, complex purifications, analytical development and validation, nanomedicines manufacturing, and global logistics / procurement.

Sam Ponticelli, Manager | 847-520-9600

 

1565 Barclay Boulevard | Buffalo Grove, IL 60089

 

Tepnel Pharma Services

Tepnel Pharma Services

Boston Booth 200

Focus on the things you can change and let go of the things that you can’t. Based in Scotland, UK and adopting a Vested Outsourcing philosophy, Tepnel Pharma Services is an independent laboratory services partner for ICH stability testing, UK/EU, global batch release testing and compendial analysis in support of small molecule and peptide drug development. Using lean manufacturing tools, we commit to
Vikki Renwick , Commercial Director | 0044 1506 424 270

 

Appleton Place Appleton Parkway | Livingston West Lothian EH54 7EZ

 

Therapure Biopharma

Therapure Biopharma

San Francisco Booth 65

Profile coming soon.

 

Address TBA

 

Triclinic Labs

Triclinic Labs

Boston Booth 202 | San Diego Booth 47 | San Francisco Booth 57

Profile coming soon.

 

Address TBA

 

Unither Pharmaceuticals

Unither Pharmaceuticals

Boston Booth 208 | 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

 

UPM Pharmaceuticals

UPM Pharmaceuticals

Boston Booth 310

UPM Pharmaceuticals is a Bristol Tennessee based contract development and manufacturing organization (CDMO) serving the pharmaceutical and biotechnology industries. UPM provides high quality pharmaceutical drug development services that include formulation development, cGMP manufacturing and packaging, analytical method development and testing from concept through commercialization. UPM is characterized by its strict sense of quality, timeliness, sound scientific fundamentals, and affordability with which we complete all our projects. We focus on drug development and manufacturing for dosages with oral routes of administration in solid forms such as capsules and tablets, and semi-solid creams and ointments.

Mary Lee Schiesz, Manager of Marketing | 423-989-7057

 

501 5th St. | Bristol TN 37620
Vetter

Vetter

Boston Booth 112

Vetter is a leading contract development and manufacturing organization (CDMO) that specializes in the aseptic filling of syringes, cartridges and vials. The company has extensive experience with biologics and other complex compounds, including monoclonal antibodies, peptides, interferons and vaccines. Collaborating with pharma/biotech clients worldwide, Vetter supports products from preclinical development through global market supply. Through its U.S. and European facilities, Vetter Development Service provides state-of-the-art support for early-stage products, with seamless transfer at Phase III to Vetter Commercial Manufacturing for large-scale production. The company offers state-of-the-art technology and innovative processes to promote product quality and maximize API yield.

Oskar Gold , Senior Vice President Key Account Management / Marketing / Corp. Communications | 847-581-6888

 

4901 Searle Parkway, Suite 300A | Skokie, IL 60077

 

Wacker Biotech GmbH

Wacker Biotech GmbH

Boston Booth 215

Wacker Biotech GmbH is “THE MICROBIAL CMO” – the partner of choice for process development and commercial manufacturing of therapeutic proteins. Based on 25 years of experience WACKER’s expertise covers projects from preclinical development to API delivery for commercial supply. WACKER’s outstanding E.coli technologies can significantly increase the bioprocess efficiency and so reduce the cost of goods. WACKER’s manufacturing lines have a capacity of up to 1,500L to flexibly serve our clients. The GMP facility in Halle received EMA approval for commercial manufacturing and was successfully inspected by the FDA in 2012. EMA approved the Jena GMP facility in 2016.

Peter Danforth , Business Development Manager | +1 517 264-8186

 

Hans-Knoell-Str. 3, 07745 Jena, Germany

 

WuXi AppTec

WuXi AppTec

Boston Booth 309 | 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 Dr. | San Diego, CA 92121

 

Yourway Transport

Yourway Transport

San Diego Booth 38 | San Francisco Booth 45

Profile coming soon.

 

Address TBA