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 Francisco 2017

Adesis
Albemarle
Alcami Corporation
Althea CMO
AMPAC Analytical Lab
Aphena Pharma Solutions
Avara Pharmaceutical Services
Avista Pharma Solutions
B. Braun Medical OEM
Berkshire Sterile Manufacturing
BioDuro
Boehringer Ingelheim
Boston Institute of Biotechnology LLC
Cambrex Corporation
CMC Biologics
Cytovance Biologics
DavosPharma
Dottikon ES America, Inc.
Eurofins Alphora
FAREVA
Flamma S.p.A.
FUJIFILM Diosynth Biotechnologies
Full Spectrum Analytics
Jubilant Chemsys
LI-COR Biosciences
Metrics Contract Services
Multipharma Inc.
Olon Ricerca Bioscience LLC
PCI Pharma Services
PCI Synthesis
Pharmatech Associates
Piramal Pharma Solutions
Quotient Clinical
Recro Gainesville
Rondaxe
SafeBridge Consultants, Inc.
Scientist
Sherpa Clinical Packaging
SHL Group
Siegfried USA, LLC
SMC, Ltd.
Therapure Biopharma
Triclinic Labs
Unither Manufacturing LLC
Yourway Transport
Sponsors: DPT Laboratories, Skyland Analytics, Symbiosis Pharmaceutical Services & PharmAssist Analytical Laboratory, Pfizer CenterOne

 

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Interested in exhibiting? Get in touch for details.

 

 

2017 Exhibitor Profiles

Adesis, Inc.

Adesis, Inc.

San Francisco Booth 19

Adesis, Inc. is a U.S.-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 47,000 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 J. Defina, Director of Business Development | 302-358-8837

 

27 McCullough Drive | New Castle, DE 19720

 

Albemarle

Albemarle

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 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

 

Althea CMO

Althea CMO

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

 

AMPAC Analytical Laboratory

AMPAC Analytical Laboratory

San Francisco Booth 07

AMPAC Analytical Lab is an expansion of AMPAC Fine Chemicals (AFC). With over 75 years of manufacturing experience. AFC recently expanded its capabilities to include contract analytical services. AMPAC Analytical specializes in analytical development and testing of cGMP Intermediates, APIs, and Drug Products.

Rosa Vais, Senior Business Development Analyst | 916-342-0363

 

1100 Windfield Way | El Dorado Hills, CA 95762

 

Aphena Pharma Solutions

Aphena Pharma Solutions

San Francisco Booth 40

Aphena is a large growing pharmaceutical contract packaging and manufacturing company. Aphena has two FDA inspected and DEA licensed facilities in the U.S. located in Cookeville, TN and Easton, MD. Aphena brings extreme value to all of our customers by offering turnkey services and one of the largest packaging capabilities of anyone in our industry. The products types Aphena is actively handling are solid dose products, ingestible liquids products, gels, creams, ointments, foams, suspensions, and lotions. DEA licensed CII-CV products - 500+ employees.

Eric Allen, Vice President of Sales and Marketing | 864-250-9512

 

1920 Fisk Road | Cookeville, TN 38506

 

Avara Pharmaceutical Services

Avara Pharmaceutical Services

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 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 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

 

Boehringer-Ingelheim

Boehringer Ingelheim Biopharmaceuticals GmbH

San Francisco Booth TBA

Boehringer Ingelheim Biopharma Contract Manufacturing is represented by its new brand Boehringer Ingelheim BioXcellence™. As a leading biopharmaceutical contract manufacturer with more than 35 years of experience it has brought more than 20 biopharmaceutical products to market. Boehringer Ingelheim BioXcellence™ offers tailor-made contract development and manufacturing services to the biopharmaceutical industry, providing the entire production technology chain from DNA to fill and finish under one roof at its facilities in Biberach (Germany), Vienna (Austria), Fremont (USA) and Shanghai (China).

Elizabeth Jaren, Business Development and Key Account Management Coordinator | 510-284-6421

 

6701 Kaiser Drive | Fremont, CA 94555

 

Boston Institute of Biotechnology LLC

Boston Institute of Biotechnology LLC

San Francisco Booth 58

As a contract research and development organization (CRDO), Boston Institute of Biotechnology, LLC, provides full spectrum services for microbial fermentation and mammalian cell culture processes. Boston Institute of Biotechnology, LLC (BIB) occupies a facility of 6,000 sf. including isolated labs for cell culture, fermentation, purification and analytical services. Our facility in Southborough, MA, within the Genetown Hotbed of Metro-Boston Area, offers flexible and adaptable lab spaces designed to meet the needs of our clients.

Mike Osborne, Director of Business Development | 860-699-9470

 

225 Turnpike Road | Southborough, MA 01772

 

Cambrex Corporation

Cambrex Corporation

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.

John Michnick, Director, Sales and Business Development | 425-210-7214

 

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

 

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 Francisco Booth TBA

DavosPharma provides manufacturing and discovery services for pharmaceutical clients through our world-wide network of experienced CROs and CMOs. Our corporate offering covers all the activities required to get a drug from conception to commercialization. DavosPharma has been filling this need since 1972, serving the pharmaceutical and life science market by providing discovery chemistry & biology, pre-clinical development, and all required CMC activities including custom synthesis of organic molecules, custom dosage formulation, and custom manufacturing of cGMP intermediates, APIs, and drug product. DavosPharma’s goal is to provide you a complete solution to your pre-clinical and custom chemistry and formulation needs

Gifford Marzoni, VP Global Pharmaceutical Development | 619-429-0120

 

600 East Crescent Ave | Upper Saddle River, NJ 07458

 

Dottikon ES America, Inc.

Dottikon ES America, Inc.

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

 

Eurofins Alphora

Eurofins Alphora

San Francisco Booth 31

Eurofins Alphora provides API technology development services for complex niche small molecules, covering pre-clinical to Phase III and commercial manufacturing. Alphora operates FDA-approved facilities totalling 51,000+ ft² including cGMP Kilo Laboratories and cGMP Plant operations, R&D and Analytical laboratories, QC/QA, as well as a separate high potency/cytotoxic facility.

Rav Mahal , Vice President, Business Development & Project Management | 905-403-1611

 

2395 Speakman Drive, Ste. 2001 | Mississauga, ON L5K 1B3 Canada

 

FAREVA

FAREVA

San Francisco Booth 50

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

 

Flamma S.p.A.

Flamma S.p. A.

San Francisco Booth 20

FLAMMA is a fully integrated CMO based in the Bergamo area (near Milan in Northern Italy) that was established in 1950. FLAMMA is a company specialized in the cGMP manufacture of APIs, NCEs, RSMs, and advanced intermediates for the pharmaceutical industry. Flamma has particular expertise in high value chiral materials specifically amino acid related materials. Flamma also manufactures specialty compounds and advanced intermediates for the nutraceutical and cosmetic industries and has several generic products. FLAMMA has three manufacturing facilities all with R&D labs. Both cGMP Italian locations (Chignolo & Isso) are regularly inspected by the FDA and AIFA. Flamma Honkai, located in Dalian, China, has a new R&D building as well as a cGMP production plant. Flamma provides security when working in China with our 100% owned, self-managed facilities that deliver results without worry. Flamma reliably supplies materials directly customers and/or delivers materials (when required) to their cGMP facilities in Italy in order to deliver the customer’s compound on-time and in the desired specifications. Flamma offers cost-effective services to customers looking for a trusted partner within China. Being a fully integrated company allows Flamma to move your compounds quickly along their journey taking into consideration all aspects necessary for the success of your project. Flamma can be of assistance for early stage pre-clinical development of small molecules as well as for large-scale commercial manufacturing. With a total reactor capacity of 450 m3 and over 450 employees, see why Flamma should be your next contract manufacturer. FLAMMA- Where It Matters Most.

Kenneth N. Drew Ph.D, Sr. Director, NA Sales & Business Development | 603-882-2602

 

Via Bedeschi 22, 24040 Chignolo d’Isola | Bergamo, Italy

 

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

 

Full Spectrum Analytics

Full Spectrum Analytics

San Francisco Booth 8

Full Spectrum Analytics is an end-to-end solutions provider specializing in Chromatography Instrumentation. We provide refurbished equipment, and are one of the leading support providers in today’s analytical instrument marketplace. We specialize in supporting Agilent Instrument Service Contracts, System Qualifications, Asset Management, LCMS QQQ Triple Quad Service, Multi-Vendor Qualifications, Preventive Maintenance, Instrument Relocation Services, HPLC / GC / Mass Spectrometers Contracts, ECD Cleaning, Pre-Owned Instrument Sales, GSA Contracts, ISO 9000, ISO 17025 Accredited, AB Sciex, Waters HPLC, Dissolution Systems, Headspace Units, CTC Gerstel LEAP, Interchim, TOC systems, GE AKTA, Bruker, Varian, Dionex and Shimadzu.

Mary Turner, Business Development Manager | 714-279-3999

 

1554 North Case Street | Orange, CA 92867

 

Jubilant Chemsys

Jubilant Chemsys

San Francisco Booth 46

Jubilant Biosys & Jubilant Chemsys (collectively Jubilant) are sister concerns of Jubilant Life Sciences. Jubilant’s services: Target Identification/Target Validation to Lead Optimization/Preclinical candidate, for multiple therapeutic areas viz; Oncology, Metabolic Disorders, CNS, Pain, Inflammation, Fibrosis and Respiratory diseases | Computational chemistry/ molecular modeling, medicinal/synthetic chemistry, scale-up (Non-GMP & GMP), structural biology, ADME-PK, in-vitro/in-vivo biology and IND enabling GLP toxicology.
Statistics: Clients- Global Top-10 Pharma | Jubilant Life Sciences ($900MM Sales Corporation) | Experience- 60+ integrated programs;12 at Lead Optimization/ IND | Multi-location: Noida, Bengaluru, India and Malvern, USA
Business models: Full Time Equivalent (FTE) | Fee For Service (FFS) | Risk share and Milestone-integrated programs

Saurabh Kapure, Associate Vice President of Business Development | 925-888-9113

 

365 Phoenixville Pike | Malvern, PA 19355

 

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

 

Metrics Contract Services

Metrics Contract Services

San Francisco Booth 38

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

 

Multipharma

Multipharma Inc.

San Francisco Booth 55

For 20 years, Multipharma has specialized in the sourcing of clinical trial materials, from comparator drugs, rescue and concomitant medication, and ancillary supplies. As your partner in Strategic Supply Planning, our global team provides integrated support from the planning stage - market research, procurement, storage, logistics, distribution, project management, material reconciliation - to forecasting. Our global footprints are in 3 continents, with 5 offices in the US, Germany, Switzerland, UK and Japan. Our network of established connections, provides you access to a large number of products and markets worldwide throughout the duration of your trial. Multipharma’s sister company, Inceptua has 20 years experience in Medicines Access and Managed Access Programmes, offering an ethical solutions-based approach to provision of unapproved medicines for patients with unmet medical needs.

Jerra Langit, Key Account Manager | 201-800-5081

 

66 Hudson Street, Ste 1 | Hoboken, NJ 07030

 

Ricerca

Olon Ricerca Bioscience LLC

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

 

PCI Pharma Services

PCI Pharma Services

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 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

 

Piramal Pharma Solutions

Piramal Pharma Solutions

San Francisco Booth 42

Piramal Pharma Solutions is a Contract Development and Manufacturing Organization (CDMO), offering end-to-end services required to bring a drug to the market place faster. We offer Pharmaceutical Development and Manufacturing solutions through collaborative partnership models and we work with our customers throughout the drug life cycle. We have created a vast network of Development and Manufacturing facilities located in North America, Europe and Asia that offers a multitude of services covering the entire drug life cycle, from Drug Discovery & Development to Commercial Manufacturing of off-patent Active Pharmaceutical Ingredients (APIs) and Finished Dosage Forms (FDFs). Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

Viacheslav Katin , Business Development Manager | +91 (0)22 30956909

 

247 Business Park, A Wing, 6th Floor | Vikhroli (W), Mumbai 400083

 

Quotient Clinical

Quotient Clinical

San Francisco Booth 53

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

 

Rondaxe

Rondaxe

San Francisco Booth 70

Rondaxe is one of the largest and most experienced international CMC consulting groups in the world. We assist both virtual pharma/biotech companies and multi-national pharmaceutical clients from early development through commercial manufacturing. Services include comprehensive CMC solutions, drug development, manufacturing and global regulatory strategies. [Re]source™ is our proprietary pharmaceutical process software to assist clients with data management, cost of goods, productivity analysis and other features.

Joel Lirot , Vice President, Business Development

 

6443 Ridings Road Suite 125 | Syracuse, NY 13206

 

Recro Gainesville

Recro Gainesville

San Francisco Booth 60

OSD manufacturing. Specializes in developing release profiles (CR, SR, DR) and IR. Capsules and tablets. Clinical material and commercial material manufacturing. Packaging for both clinical and commercial supplies. DEA regulated drugs accepted.

Lettie Kirk , Sr Sales Manager

 

1300 Gould Drive | Gainesville, GA 30504

 

SafeBridge Consultants, Inc.

SafeBridge Consultants, Inc.

San Francisco Booth 49

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 Conner , Business Development Assistant | 212-727-0717 x 217

 

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

 

Scientist

Scientist

San Francisco Booth 6

Scientist.com is on a mission to empower and connect researchers worldwide through our online marketplaces with a faster, leaner, and "innovation-centric" approach for acquiring custom services. The original pioneer and industry leader in this space, Scientist.com has multiyear partnerships with 14 of the top 25 pharmaceutical companies and the NIH.

Wyatt Hinshaw , Business Development Manager | 1-858-699-1978

 

125 N. Acacia Ave. | Suite 111 | Solana Beach, CA 92075 USA

 

Sherpa Clinical Packaging

Sherpa Clinical Packaging

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

 

SHL Group

SHL Group

San Francisco Booth 63

SHL designs, develops and manufactures advanced drug delivery devices including auto injectors and pen injectors. With locations in Taiwan, Sweden and the US, our experienced engineers and designers develop product enhancements and breakthrough drug delivery solutions for pharma and biotech clients globally. Significant investment in R&D has enhanced our broad pipeline of “next generation” drug delivery systems. These innovative devices include a range of disposable and reusable injectors with fixed or variable dosing, enhanced precision and the ability to accommodate high viscosities. Additionally, SHL provides final assembly, labeling and packaging services for leading pharmaceutical and biotech companies across the globe.

Jamie Gould, Business Development Manager | 954-725-2057

 

588 Jim Moran Boulevard | Deerfield Beach, FL 33436

 

Siegfried USA, LLC

Siegfried USA, LLC

San Francisco Booth 14

Siegfried is your preferred partner for complete integrated drug substance and drug product services with production capabilities worldwide. Our professionalism is pivotal for your project throughout the entire life cycle. Creating and manufacturing formulations is our passion. We work closely with customers to develop and optimize innovative chemical processes with broad capability adding benefit and value. Siegfried has chemical manufacturing multipurpose cGMP sites located in: Zofingen and Evionnaz, Switzerland; Minden, Germany; Saint-Vulbas, France; Pennsville, New Jersey (USA); and, Nantong, China. Our drug product manufacturing sites are located in Zofingen, Switzerland (Pilot), Irvine, California, Malta and Hameln, Germany.

Sandy Cernick, VP Marketing | 412-427-0757

 

33 Industrial Park Road | Pennsville, NJ 08070

 

SMC, Ltd.

SMC, Ltd.

San Francisco Booth 64

SMC Ltd. provides contract manufacturing of single-use devices for the health care, pharmaceutical and diagnostics industries. With 700,000 sq. ft. dedicated to medical manufacturing, SMC provides full product services from initial concept through final packaged device; including: program management, design and development, product manufacturing, clinical manufacturing, electronics integration, and global supply chain management.

 

330 SMC Drive | Somerset, WI 54025

 

Therapure Biopharma

Therapure Biopharma

San Francisco Booth 65

Contract manufacturing of biologics is more than having superior technology - it's having experienced people who are passionate, responsive and committed to developing and manufacturing your biotherapeutics to improve patient care. Therapure Biomanufacturing is a biopharmaceutical CDMO specializing in sophisticated biologic products at its 130,000 sq ft, cGMP facility. Our expertise includes development services (cell line, upstream & downstream processes and analytical methods) as well as cGMP manufacturing (upstream processing, downstream purification and aseptic fill/finish).

Christopher Jackson, Associate Marketing Manager | 905-286-6270

 

2585 Meadowpine Blvd | Missisauga, ON, L5N 8H9

 

Triclinic Labs

Triclinic Labs

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 Francisco Booth 27

Unither Pharmaceuticals’ affordable and covenient 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

 

Yourway Transport

Yourway Transport

San Francisco Booth 45

Yourway Transport BioPharma Services offers sponsors access to a global supply chain network of strategically positioned facilities to support their clinical trials. This network is supported via a proprietary inventory system offering visibility to all study transactions. In addition, we offer support in clinical supply chain management, IRT, cold chain packaging, distribution, bio sample management & reverse logistics. The Transport Services Division has set the standard for quickness and personalized service within the global pharmaceutical industry. Expertise includes ambient and cold chain premium courier services, consultation on global requirements, customs clearance, sourcing and provision of shipping supplies and project management.

Frank Di Stefano, VP of Sales BioPharma Services | 858-334-8479

 

6681 Snowdrift Road | Allentown, PA 18106