Dedicated Project Management



Similar documents
Highly Potent APIs The right platform, people and procedures for successful development and manufacturing

NEW CHEMICAL ENTITIES

Specific Challenges in Large-Scale Manufacturing of Peptide as API s Presentation at TIDES Conference, Las Vegas, April 25 29, 2004

EuroPeptides 2014: Workshop Considerations for Peptide Contract Manufacturing: Case Study on Scale-up Considerations

C 5. chemical development contract research custom synthesis cgmp API manufacturing commercial production. Welcome to

Challenges in Industrial Production of Peptides. Dr. Daniel Bourgin Director of Sales & BD LCM-TIDES, Lonza Ltd. Basel, Switzerland

LifeTein in Industrial Production of Therapeutic Peptides. Phil Moore, PhD Director of Business Development LifeTein LLC, NJ, USA

colorado EXPERTS TAKING CARE

Brand Quality with Asian Advantages

Valentina Gualato, Ph.D. Process Development Scientist

Custom Synthesis. Reliable, Flexible and Competitive T H E R I G H T C H E M I S T R Y

Custom Synthesis. Reliable, Flexible and Competitive THE KEY SOLUTION PROVIDER A FINE CHEMICAL COMPANY. About ISOCHEM

Providing Trusted and Innovative Solutions t o the Life Science Communities

LFB GROUP & SANOFI combine their bioproduction capabilities to provide integrated CMO services for biopharmaceuticals

A novel method for the synthesis of peptides

Peptide purification strategies

BIOTECH MANUFACTURING SOLUTIONS 4 YOUR SUCCESS. a Novartis company

LFB GROUP & SANOFI combine their bioproduction capabilities to provide integrated CMO services for biopharmaceuticals

Facility construction and start up for commercial scale manufacturing of monoclonal antibodies - A case study

1) Technical informations. - a) How does it work? - b) Purification - c) Quality Control. 2) Standard synthesis

CUSTOM PEPTIDE SYNTHESIS AT BACHEM

How To Make A Drug From A Peptide

Guidance for Industry

Welcome to the ChemCon Company Presentation: 6 Steps to Success for our Customers!

The Peptides Vol. 2: Analysis, Synthesis, Biology: Special Methods in Peptide Synthesis

2010 European Amino Acid Derivatives Product Line Strategy Award

Biotechpharma company profile

Non-GMP and GMP Services From Lab Scale R&D to Bulk API Production

USP's Therapeutic Peptides Expert Panel discusses manufacturing processes and impurity control for synthetic peptide APIs.

China has become the world s factory, second only to the USA in terms of CO 2 emissions among major industrial countries.

GEA Niro Pharmaceutical GMP Spray Drying facility. Spray drying process development and contract manufacturing. engineering for a better world

Sosei acquires Jitsubo, a leading Japanese peptide technology company

Liquids Suspensions Gels

Focus XC. Ultimate Fully Automated Peptide Synthesizer with Sonication and Heating Options

Pharmaceuticals Production Services Boehringer Ingelheim. Our expertise in world-class contract manufacturing for your success

TENDER DOCUMENT PURCHASING EQUIPMENT FOR PEPTIDE SYNTHESIS

Automated Fast-Bead Synthesis of Small Peptides

Working with ICH Quality Guidelines - the Canadian Perspective

Catalent Biologics & Clinical Supplies The SMART Solution

Combinatorial Chemistry and solid phase synthesis seminar and laboratory course

Eden Biodesign ebook Monoclonal Antibody Production: Building the Platform

MANAGING THE COMPLEXITIES OF GLOBAL PHARMACEUTICAL SOURCING

ICH guideline Q11 on development and manufacture of drug substances (chemical entities and biotechnological/ biological entities)

Experimental procedures. Solid phase peptide synthesis (SPPS)

Aspects of industrial purification of peptides using large-scale chromatography. Lars Andersson and Jonas Persson

Syngas Purification Units

Liquid II Cell Culture Media Manufacturing Plant. Overview Facilities Water for Injection Sterile Environment Media Handling Cleanroom Interior

Outline. Market & Technology Trends. LifeTein Technology Portfolio. LifeTein Services

Reagents, Tools, and Services for Pharma Manufacturing. GMP Grade Advanced Intermediates, and Customized Solutions

INDUSTRY OVERVIEW. Our business segments. (ii) Global drug development service market Preclinical drug development services

DEMTROL High Performance Crude Oil Demulsifier Bases FPO. Setting the Standard for Emulsion Breaking in Production Operations

ICH Public Meeting. Joseph C. Famulare. October 2, Acting Deputy Director Office of Compliance CDER / FDA Office of Compliance

From Research Services and Process Development to GMP Manufacturing

Regulatory Affairs Graduate & Postgraduate Program. Novartis Pharma AG Novartis Animal Health AG

Syllabus. 1. Occurrence and Functions of Peptides in Nature and Every Day Life hormones, neurotransmitters, therapeutics, artificial sweetener,

Drug Information Journal, Vol. 33, pp , /99

The Importance of Developing a High Yield of Product

Your partner in immunology

Peptide Synthesis Zheng Miao* and Zhen Cheng

Large Scale Solid Phase Organic Synthesis

Overview of Drug Development: the Regulatory Process

Harmonizing Change Control Processes Globally

An Industry White Paper

C&EN Webinar. Success in Highly Potent API Manufacturing

Selvita Integrated drug discovery collaborations

Preparing for the Pre-Approval Inspection What to do Before the FDA Arrives. Barry A. Friedman, Ph.D. Consultant

Green Principles Atom Economy Solventless Reactions Catalysis

Extraction of Caffeine from Energy Drinks

Guidance for Industry

Hamari Chemicals, Ltd.

SELECT Hg Ultra-purification of mercury from natural gas

Continuous manufacturing moving towards real-time release. Creating innovations for the pharmaceutical industry. siemens.

KMS-Specialist & Customized Biosimilar Service

White Paper. By Jack Vinson, PhD, Product Manager, Batch Process Development, Aspen Technology

Antibody Services. Best Guarantees in the Industry! Monoclonal Antibody Services. Polyclonal Antibody Services. Express Antibody TM Services

Illumina Sequencing Technology

Library Guide: Pharmaceutical GMPs

BioResearch. RAFT 3D Cell Culture Kit Protocol

Custom Antibodies. Animals Chicken, Goat, Guinea Pig, Mouse, Rat, Rabbit, etc. Antibody Identification Dot blot ELISA IHC Western blot

Short Peptide Synthesis

CEM, First in Microwave Peptide Synthesis

Guidance for Industry. Monoclonal Antibodies Used as Reagents in Drug Manufacturing

Accelerating drug development to FTIH: Potential of new expression technologies

Workshop on process validation

Bayer Technology Services

Use of the ambr 250 in combination with high-throughput design and analysis tools for rapid, scalable USP development

l 4-minute cycle time l 90% solvent reduction Remarkably fast Automated Microwave Peptide Synthesizer

Guidance for Industry

Luca Romagnoli, Ph.D. Business Development Manager

Ph.D. Science & Engineering Positions. Wilmington, DE. Analytical Sciences Wilmington, DE. Sciences Wilmington, DE.

Presented at: Jefferies 2015 Global Healthcare Conference

FDA STAFF MANUAL GUIDES, VOLUME I - ORGANIZATIONS AND FUNCTIONS FOOD AND DRUG ADMINISTRATION OFFICE OF GLOBAL AND REGULATORY OPERATIONS AND POLICY

Quality. Now Certified to ISO 9001:2008

2Technical Support 3Formulation Development 4Proof of Concept 5 GMP Services 6Advanced Drug Delivery 1EUDRAGIT Products Evonik. Power to create.

Una nueva plataforma para la producción de vectores lentivirales para preclínica y bajo cgmp

MAB Solut. MABSolys Génopole Campus 1 5 rue Henri Desbruères Evry Cedex. is involved at each stage of your project

Transcription:

Peptides

Dedicated Project Management At Lonza, we are committed to our customers success, so it is our mission to help your product reach its full potential. We pride ourselves on delivering high-quality, flexible service that is both responsive and pro-active. Every program at Lonza is assigned a dedicated Customer Project Manager who leads the project team to deliver results while anticipating and resolving unforeseen challenges. This internal advocate coordinates all activities associated with your project and continually updates you on its progress. Their goal is to drive the project to make sure the agreed upon activities, timelines, and budget are met to your complete satisfaction.

What Makes Us Different? With over 30 years in peptide manufacturing and development, we pride ourselves on providing customers a tailored approach built around a unique peptide competency that helps your product reach its full potential. Our scientists and dedicated project managers are able to tap into over 100 years of Lonza chemistry knowhow and a 25-year biotechnology track record. Combine this with versatile capabilities and scales, quality and regulatory expertise, new innovations and continuous improvement, and our ability to secure supply and you ve got a peptide provider you can trust. Versatile Capabilities, Scales Recombinant, solid- and liquid-phase technologies Milligram to ton quantities Upstream and downstream expertise Quality & Regulatory Expertise Highest quality manufacturing Strong regulatory track record DMF / CMC support Successful filing of IND s and NDA s Wide experience with FDA and EMEA Security of Supply Financially sound Backward integrated Multi-site offering Strategic global sourcing Innovation & Continuous Improvement Investments and collaboration for cutting-edge technology Operational excellence Unique manufacturing pathways Leverage Lonza-wide Know-how Highly potent APIs Peptide conjugates Microreactors Extensive life science network

A World of Experience Our peptide experience began 30 years ago when the first solidphase peptides were produced at our Braine-l Alleud facility in Belgium. Since then, we have worked hand-in-hand with both large and emerging pharmaceutical companies to develop and manufacture hundreds of peptides, using all three peptide technologies. Today, we re one of the world s leading producers of custom peptides, with four production sites, over 400 dedicated professionals, a strong manufacturing track record and a complete range of R&D services. Full Range of R&D Services Feasibility studies Process development Process optimization Process validation Analytical development and methods validation Stability studies Regulatory support Broad Technology Set Solid-Phase Synthesis (SPPS) FMOC chemistry Up to 50 amino acids Natural and synthetic amino acids Liquid-Phase Synthesis (LPPS) BOC and Fmoc chemistry Short and medium peptides Hybrid Approach Production of various fragments on solid support (resin) and subsequent condensation of cleaved fragments in liquid-phase Recombinant DNA Technology By fermentation/concatemer approach State-of-the-Art Facilities Our cutting-edge facilities and broad technology experience means we can offer a full range of cgmp production strategies depending on your peptide s structural complexity. Additionally, we have a broad array of synthesis, purification, isolation, and analytical equipment as well as support infrastructure to find an optimal solution for your immediate and long-term peptide needs. Europe Braine, Belgium Solid-phase and liquid-phase technology Kouřim, Czech Republic Recombinant DNA technology Visp, Switzerland Solid-phase, liquid-phase and recombinant DNA technology Asia Nansha, China Solid-phase and liquid-phase technology Upstream & Downstream Equipment Solid-Phase Synthesizers from 50mL to 1 600L Cleavage systems Liquid-Phase Vessel sizes range from 10L to 2 800L Cyclization lines Recombinant DNA Technology Microbial production in vessels from 15m3 to 75m 3 Purification Large-scale HPLC (15 to 60cm) Mid- and Small-scale HPLC Various packing material options Up to 100 bar Quality Control (IPC methods & HPLC) Isolation / Filtration Lab-scale lyophilization (freeze dryers) Industrial-scale lyophilization (up to 200kg ice/day) Lab- and pilot-scale spray drying Centrifuges Agitate and static plate filters Filter-dryer Extraction devices Hydrogenators

Strategic Support Infrastructure Streamlined (worldwide) sourcing Raw materials in rail-tank-cars Tank-farms No open handling Adequate warehousing Recycling systems Exhaust gas treatment Waste disposal Total Life-Cycle Management At Lonza, we have the experience and facilities to take a new chemical entity from feasibility studies and process development through validation and scale-up all the way to market penetration, commercial leadership, and off-patent protection. Whether you need us to provide simple R&D work, complete process redevelopment, or any scale of manufacturing we are prepared to help step-by-step from day one. Product Offering Early intermediates (GMP / non-gmp) Advanced peptide intermediates, including chemical modification (e.g. PEG, disulfide bridge, etc.) Bulk actives / drug substance Generic peptides

We welcome the opportunity to help you tackle any peptide challenge. From early-stage development through in-market supply, we are prepared to meet your immediate and long-term peptide needs with innovative and trusted solutions. Please don t hesitate to call us for a chat about how we can help. Lonza Ltd Muenchensteinerstrasse 38 CH-4002 Basel, Switzerland Tel +41 61 316 81 11 contact@lonza.com Lonza Inc. 90 Boroline Road Allendale, NJ 07401 Tel +1 201 316 9200 contact.us@lonza.com www.lonza.com The information contained herein is believed to be correct and corresponds to the latest state of scientific and technical knowledge. However, no warranty is made, either expressed or implied, regarding its accuracy or the results to be obtained from the use of such information and no warranty is expressed or implied concerning the use of these products. The buyer assumes all risks of use and/or handling. No statement is intended or should be construed as a recommendation to infringe any existing patent. 2009 Lonza Ltd, Basel Switzerland Printed in the USA