Drug Substance

Drug Substance
Product Description

BioDuro-Sundia’s Drug Substance manufacturing services support production of small molecule APIs, RSMs and intermediates--both GMP and non-GMP .  We provide a full range of production scale, supporting all stages of drug substance development through IND submission.  Fully integrated CMC services boasts a proven track record of over 100 clients. With over 20 IND & Generic DMF Filings, our team has deep experience in complex Sugar Chemistry & heterocyclic compound manufacturing.
Facility Overview

  • Manufacturing facilities & storage – 20,000 ft2²
  • Capability of wastewater disposal: 50 tons/day
  • Utility: Saline water cooling, compressed air, soft water
  • 120 research fume hoods in Process Lab
  • Non GMP kilo scale lab: 17 reactors from 50 – 100L
  • cGMP kilo lab: 5 reactors from 100 – 200L
  • Temp reaction capability: 800C℃ – 2300C℃
  • Pressure reaction upto 1mPa (120 psi)
  • Clean room for API production
  • Non-GMP pilot plant with 20 reactors from 300L – 5000L
  • Chromatography column/Separation System: DAC 150 & DAC 300

BioDuro

  • US
  • 2018
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
Contract Service

BioDuro

  • US
  • 2018
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
Contract Service

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BioDuro resources (13)

  • Video Company Video - Integrated Drug Discovery, Development and Manufacturing at BioDuro-Sundia

    BioDuro-Sundia is your partner for accelerating drug discovery, development and manufacturing--from molecule to market. Find out more at http://www.bioduro-sundia.com. 
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    BioDuro-Sundia’s Drug Substance manufacturing services support production of small molecule APIs, RSMs and intermediates--both GMP and non-GMP .  We provide a full range of production scale, supporting all stages of drug substance development through IND submission.
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    BioDuro-Sundia’s process development services support drug substance production,  providing an efficient path to manufacture API or intermediates. Our extensive services support production of API for GLP toxicology studies, IND-enabling studies, clinical studies, and commercialization efforts.  
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    BioDuro’s analytical team is well-integrated into the formulation and manufacturing programs to facilitate and accelerate the development of the analytical methods and testing of prototypes, raw materials and drug products. Sharing knowledge of the formulation and the manufacturing process results in analytical data that is scientifically sound and project support that is well-coordinated and timely.

    Experienced and dedicated development and QC chemists at BioDuro are committed to the highest levels of technical quality and GMP compliance.
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    Bioavailability enhancement for poorly soluble compounds
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  • Webinar Webinar - Protein Degraders

    Since 2015 the field of targeted protein degradation has rapidly emerged, offering opportunities for novel pharmacological interventions in ways impossible to achieve with traditional small molecule inhibitors. This webinar focuses on cutting-edge drug discovery using protein degraders, such as PROTACS, in diverse therapeutic areas. Attendees can expect to learn about recent strategies toward development of orally bioavailable protein degrader drug candidates—PROTACs and beyond.