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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2018 Exhibitors by Show

Boston

AGC Biologics
Albemarle
Avista Pharma Solutions
Berkshire Sterile Manufacturing
Boston Analytical
Coating Place
CordenPharma International
Cytovance
Dottikon Exclusive Synthesis
Emergent Biosolutions
IDBS
Jubilant Chemsys
Lifecore Biomedical
LSNE
Metrics Contract Services
Myoderm
Olon Ricerca Bioscience LLC
PCI Pharma Services
PCI Synthesis
PharmAssist Analytical Laboratory
Pharmatech Associates, Inc.
Procos SpA
Quotient Sciences
Raffles PharmaTech
Ropack Pharma Solutions
Safebridge Consultants, Inc.
Sherpa Clinical Packaging
SynConnection
Sponsors: Cambrex

 

Philadelphia

Alliance Contract Pharma
Avista Pharma
Berkshire Sterile Manufacturing
Boston Analytical
Emergent Biosolutions
Lifecore Biomedical
Paragon BioServices
PharmAssist Analytical Laboratories
Quotient Sciences
Safebridge Consultants, Inc.
Sherpa Clinical Packaging
Sponsors: Cambrex

 

San Deigo

Albemarle
AMPAC Analytical Lab
Avista Pharma
Boston Analytical
CordenPharma International
Dottikon Exclusive Synthesis
FAREVA
Lifecore Biomedical
Metrics Contract Services
Olon Ricerca Bioscience LLC
PCI Synthesis
PharmAssist Analytical Lab
Pharmatech Associates, Inc.
Procos SpA
Quotient Sciences
Raffles PharmaTech
Sherpa Clinical Packaging
SynConnection
Sponsors: Cambrex

 

San Francisco

AGC Biologics
Avista Pharma
Boston Analytical
Cytovance Biologics
Dottikon Exclusive Synthesis
FAREVA
FUJIFILM Diosynth Biotechnologies
Jubilant Chemsys
Lifecore Biomedical
Myoderm
Olon Ricerca Bioscience LLC
Paragon BioServices
PharmAssist Analytical Laboratory
Pharmatech Associates, Inc.
Quotient Sciences
Safebridge Consultants, Inc.
Sherpa Clinical Packaging
Sponsors: Cambrex

 

 

Interested in exhibiting? Get in touch for details.

 

 

2018 Exhibitor Profiles

AGC Biologics

AGC Biologics

Boston | San Francisco

AGC 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. AGC Biologics also offers license to CHEF1™, a proprietary CHO cell line expression technology platform. Visit agcbio.com to learn more.

Kim Yang, Director of Global Marketing | 202-725-4202

 

22021 20th Avenue SE | Bothell, WA 98021

 

Albemarle

Albemarle

Boston | San Diego

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

 

Alliance Contract Pharma

Alliance Contract Pharma

Philadelphia

Alliance Contract Pharma is a contract development and manufacturing organization (CDMO) providing contract analytical and manufacturing services to the pharmaceutical industry. Our FDA and DEA registered GMP facility allows us to formulate, develop and scale your drug product from pre-clinical through commercial manufacturing. Our manufacturing capabilities include expertise in the development and manufacturing of most solid, semi-solid, cream, liquid and suspension dosage forms. We are equipped to handle two unique manufacturing processes for the formulation and development of poorly soluble drugs including liquid filled capsules and wet milling. In addition, our ISO7/ISO 8 manufacturing area allows for the development and manufacturing of high potent compounds including injectable vial filling (post-sterilized). Our Analytical support our manufacturing capabilities and include method development, product release and ICH stability testing. Our unwavering commitment is to offer to you an environment and work ethic built upon core quality values of the highest degree, enabling you to successfully formulate, develop and scale your drug product in a timely manner. At all times we will work with you. Our goal is to continually advance the development and success of your drug product at every stage of development and at each milestone in the drug development process. No exceptions!

Stephen L. Schweibenz, President | 215-256-5920

 

1510 Delph Drive | Harleysville, PA 19438

 

AMPAC Analytical Laboratory

AMPAC Analytical Laboratory

San Diego

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

 

Avista Pharma Solutions

Avista Pharma Solutions

Boston | Philadelphia | San Diego | San Francisco

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

 

Berkshire Sterile Manufacturing

Berkshire Sterile Manufacturing

Boston | Philadelphia

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

 

Boston Analytical

Boston Analytical

Boston | Philadelphia | San Diego | San Francisco

Profile coming.

Debra Carbone, Marketing Coordinator | 603-212-5307

 

14 Manor Parkway | Salem, NH 03079

 

Coating Place

Coating Place

Boston

Profile coming.

Fred Schulze, Vice President, Technical Sales | 817-477-2766

 

200 Paoli St | Verona, WI 53593

 

CordenPharma International

CordenPharma International

Boston | San Deigo

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 U.S. organized under five technology platforms – Peptides, Oligonucleotides, Lipids & Carbohydrates, Injectables, Highly Potent & On-cology, Small Molecules, Antibiotics - CordenPharma experts translate complex ideas at any stage of development into high-value products.

Abby Thompson, Global Marketing Communications Manager | 617-909-5312

 

2075 55th St | Boulder, CO 80301

 

Cytovance Biologics

Cytovance Biologics

Boston | San Francisco

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

 

Dottikon ES America, Inc.

Dottikon Exclusive Synthesis

Boston | San Francisco

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

 

Emergent Biosolutions

Emergent Biosolutions

Boston | Philadelphia

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

 

FAREVA

FAREVA

San Diego | San Francisco

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

 

IDBS

IDBS

Boston

Profile coming.

Chelsea Hyde, Field Market Manager | 978-302-3613

 

285 Summer Street, Floor 5 | Boston, MA 02210

 

FUJIFILM Diosynth Biotechnologies

FUJIFILM Diosynth Biotechnologies

San Francisco

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

 

Jubilant Chemsys

Jubilant Chemsys

Boston | San Francisco

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

 

Lifecore Biomedical

Lifecore Biomedical

Boston | Philadelphia | San Diego | San Francisco

Do you have a difficult solution to aseptically fill? Lifecore Biomedical, LLC, has over 25 years of experience in cGMP compliant aseptic filling (vials and syringes) of difficult to fill, high viscosity pharmaceuticals. Lifecore has a flexible, robust quality system which supports your clinical development and commercialization efforts. Lifecore provides customized formulation, filtration, filling, and packaging services from pre-clinical development through commercial production. Contact us for more information or to request a quote www.lifecore.com.

Rebecca Sabasky, New Business Development Manager | 952-368-6321

 

3515 Lyman Blvd | Chaska, MN 55318

 

LSNE

LSNE

Boston

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 pro-viding 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 mate-rial 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 Sales and Marketing | 781-777-2687

 

23 Commerce Drive | Bedford, NH 03110

 

Metrics Contract Services

Metrics Contract Services

Boston | San Diego

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

 

Myoderm

Myoderm

Boston | San Francisco

Profile coming.

Maryanne L. Walsh, Director, Marketing & Sales Operations | 610-233-3311

 

48 E. Main St | Norristown, PA 19401

 

Ricerca

Olon Ricerca Bioscience LLC

Boston | San Diego | San Francisco

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

 

Paragon BioServices

Paragon BioServices

Philadelphia | San Francisco

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.

Philip Willis, VP, Business Development & Principal Scientist | 410-975-4065

 

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

 

PCI Pharma Services

PCI Pharma Services

Boston

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

Boston | San Diego

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 | Philadelphia | San Diego | San Francisco

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 | 607-373-2910

 

3392 State Highway, 8 South | New Berlin, NY 13843

 

Pharmatech Associates

Pharmatech Associates

Boston | San Diego | San Francisco

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

 

Procos SpA

Procos SpA

Boston | San Diego

Profile coming.

Alicia Xaka, Manager, Business Development | 631-332-8175

 

Via G. Matteotti 249 | 28062 Cameri, Italy

 

Quotient Clinical

Quotient Clinical

Boston | Philadelphia | San Diego | San Francisco

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

 

Raffles PharmaTech

Raffles PharmaTech

Boston | San Diego

Profile coming.

Andrew T. Phillis, Ph.D, VP of Business Development | 86 135-0017-5701

 

:No 3, Binhai 10th Road North Shihua Dadao Middle, Daya Bay, Huizhou, Guangdong, China

 

Ropack Pharma Solutions

Ropack Pharma Solutions

Boston

Profile coming.

Paul Dupont514-535-7000

 

10801 Mirabeau | Montreal H1J1T7 Canada

 

SafeBridge Consultants, Inc.

SafeBridge Consultants, Inc.

Boston | Philadelphia | San Francisco

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

 

Sherpa Clinical Packaging

Sherpa Clinical Packaging

Boston | Philadelphia | San Diego | San Francisco

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

 

SynConnection

SynConnection

Boston | San Diego

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 midsized 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.

Iver J. Berry, President | 732-780-5021

 

1565 Barclay Blvd | Buffalo Grove, IL 60089