cordenpharma switzerland...cgmp manufacturing facility with over 25 years of experience in the...

6
SWITZERLAND EXPERTS TAKING CARE CORDEN PHARMA CordenPharma Switzerland Eichenweg 1 4410 Liestal Switzerland Phone +41 61 906 59 59 Fax +41 61 906 59 58 [email protected] www.cordenpharma.com

Upload: others

Post on 19-Jul-2020

3 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: CordenPhARmA Switzerland...cGMP manufacturing facility with over 25 years of experience in the production of pharmaceutical ingredients including synthetic lipids, peptides, carbohydrates

SwitzerlandEXPERTS TAKING CARE

CordenPhARmA

CordenPharma Switzerland Eichenweg 14410 LiestalSwitzerland

Phone +41 61 906 59 59Fax +41 61 906 59 58

[email protected]

www.cordenpharma.com

Page 2: CordenPhARmA Switzerland...cGMP manufacturing facility with over 25 years of experience in the production of pharmaceutical ingredients including synthetic lipids, peptides, carbohydrates

Our History• 1987-FoundedasSygenaAGfocusingonlipidandaminoacidchemistry

• 1994-GenzymeCorporationacquiredSygenaAGfortheGMPmanufactureof APIsandhigh-valuepharmaceuticalexcipients

• 1999-SygenaofficiallychangeditsnametoGenzymePharmaceuticals

• 2011-GenzymePharmaceuticalsacquiredbyICIGtobecomeCordenPharmaSwitzerland

Cordenpharma SwitzerlandCordenPharmaSwitzerland,locatedinLiestalnearBasel,isacGMPmanufacturingfacilitywithover25yearsof experienceintheproductionof pharmaceuticalingredientsincludingsyntheticlipids,peptides,carbohydratesand

othercomplexsmallmolecules.CordenPharmaSwitzerlandisadditionallyanindustry-recognizedleaderinthemanufacturingof aminoacidderivativesandpseudoprolinedipeptidessuitablefortheGMPproductionof

peptideAPIs.CordenPharmaSwitzerland’s chemists are experts indevelopingandprovidingscalableprocesses,analyticalcontrolsandfullDMF/IND/IMPDsupportforthemanufactureof complexmolecules.

> 25 Years of Experience

Your Cmo partner

us Compliance Worldwide•cGMP certification -

API manufacturing and Analytical Testing

•US-FDA – 2000, 2004, 2007, 2011

•Swissmedic – bi-annually - most

recently April 2011, April 2013

•Numerous customers from all over the world

Page 3: CordenPhARmA Switzerland...cGMP manufacturing facility with over 25 years of experience in the production of pharmaceutical ingredients including synthetic lipids, peptides, carbohydrates
Page 4: CordenPhARmA Switzerland...cGMP manufacturing facility with over 25 years of experience in the production of pharmaceutical ingredients including synthetic lipids, peptides, carbohydrates

Core CapabilitieS•SyntheticPhospholipids•Peptides•Conjugates•Carbohydrates•SmallMolecules•ProprietaryBuildingBlocks(smallpack) -SyntheticPhospholipids -AADs -PseudoprolineDipeptides

what we do Custom manufacturingof apis

Lipids, Peptides & Carbohydrates

CordenPharmaSwitzerlandistheleaderintheproductionof fullysyntheticglyceroandsphingolipids,whicharehighlypurifiedsinglecompoundsproducedinbulkquantitieswithconsistentbatch-to-batchquality.UsedascriticalformulationexcipientsandAPIsinanumberof approvedparenteralsandpulmonarydeliveredtherapeutics,ourlipidsareavailableinsmallquantitiesforResearch&Development.CordenPharmaSwitzerlandisalsoapreferredpartnerforthecustommanufactureof cationiclipidsusedinliposomaldeliveryof oligonucleotide-basedactiveingredients.

Ourcorecompetenciesfurthermoreincludesolution-phaseand/orsolid-phasepeptidechemistry.Within-housedevelopmentandmulti-tonproductioncapabilitiesforchiralbuildingblocks,unusualandnaturalaminoacidderivatives,ourcost-effectivepeptideAPImanufacturingensuresthebestpossiblecontrolof supplychainandregulatoryrequirements.Inaddition,wepioneeredtheproductionanduseof pseudoprolinedipeptidesbuildingblocks,whicharepowerfultoolsforbypassingchallengesassociatedwiththesynthesisof “difficultsequences”and long peptides.

CordenPharmaSwitzerlandhasadditionallydevelopedexpertiseintheefficientmanufactureof carbohydrates(mono-andoligosaccharidebuildingblocksandchemically-definedglycans)onamulti-kgscale.Combinedwithourstrongexpertiseinfully-syntheticlipid,peptideandaminoacidchemistry,CordenPharmaSwitzerlandisuniquelypositionedtomanufactureglycoconjugatessuchasglycosylamino-acids,glycopeptidesorglycolipids.

OurSwissfacilitymaintainsanindependentQualityAssurancegroupandQualityControllaboratories,ensuringseamlesscustomersupportincriticaldevelopmentareassuchasanalyticaldevelopment&validation,cleaningmethoddevelopment&validation,stabilitystudiesandthefilingandmaintenanceof documentationsuchasUS-DMFs,EDMFsandothers.

we serve an expansive global customer base from start-up to large biotech or pharma with complex development and commercial products, r&d samples and reference standards in various stages.

Page 5: CordenPhARmA Switzerland...cGMP manufacturing facility with over 25 years of experience in the production of pharmaceutical ingredients including synthetic lipids, peptides, carbohydrates
Page 6: CordenPhARmA Switzerland...cGMP manufacturing facility with over 25 years of experience in the production of pharmaceutical ingredients including synthetic lipids, peptides, carbohydrates

teChnologieS / proCeSSeS Inadditiontolipid,peptideandcarbohydratechemistry,CordenPharmaSwitzerlandhasprovenscale-upexperienceinabroadrangeof chemicaltransformationsincludingbutnotlimitedto:

•Acetylation

•Acylation

•Enantioselectivesynthesis

•CatalyticHydrogenation(homogeneous,heterogeneous)

•SuzukiCoupling

•SharplessEpoxidation

•Grignardreaction

•Mitsunobureaction

•Organometallicreactions

•Phosphorylation

•Polymerisation

•Oxidation(Swern/Tempo)

•Wittigreaction

equipment detailSEquipment for pilot batches and commercial production

•Kilo-labsuitesforsmall-scalecGMPrequirements

•Equipmentcapacityrangingfrom20to160L

•Reactorsuites

-Reactorcapacity:60to2500L

-Temperaturerange:-90°Cto160°C

•Dryingsuites

-Conicaldryer

-Vacuumtraydryers

•Milling/Screeningsuite

•Large-scalechromatography

Specialized Purification & Isolation Equipment

•PreparativeHPLCequipment(reversedphase;normalphase)

•Lyophilization

CapaCitieSReaction vessels (multi-purpose and dedicated equipment)

•Pilotplantforkg-scale

•cGMPproductioninvesselvolumesrangingfrom20Lto2500L

CmC developmentcGMP Manufacture

•Experiencedprojectmanagersforseamlesstechnologytransfer,routescoutingandprocessdevelopmentforexclusiveNCEs,excipientsandhigh-valueintermediates

•Manufacturingprocessvalidationstudies

•Clinicaltrialandcommercialmaterialsupply

Analytical Support

•Analyticalmethoddevelopmentandvalidationforin-processandreleasetesting

•Impurityprofilecharacterization

•Referencestandardproduction,qualificationandsupplytocustomers

•Cleaningmethoddevelopment&validation

Quality & Regulatory Support

•StabilitytestingaccordingtoICHguidelines

•Forceddegradationstudies

•Filingandmaintenanceof US-DMFs,EDMFsandothers

•Authoringof responsedossierstoauthorities