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piCHEM Forschungs- und Entwicklungs GmbH offer service "GMP Production"

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Basic Information

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Trade Type

Offer Service

Service Name

GMP Production

Specifications

  • Service Category: Custom/exclusive synthesis of the active pharmaceutical ingredient (API) "GMP Production" by piCHEM Forschungs- und Entwicklungs GmbH for pharmaceutical manufacturers.
  • Regulatory Certification: Production facilities are inspected and approved by national authorities and the US FDA, with peptide manufacturing in compliance with ICH guidelines.
  • Capacity Scale: A 1,200 m² production facility supports GMP manufacturing of APIs from milligram to several-hundred-gram scale.
  • Geographic Coverage: Geographic coverage is not detailed in the listing beyond the supplier serving regional and international pharmaceutical customers.
  • Lead Time: Lead time is not specified in the listing; it is confirmed directly with the supplier at the time of order.

Other Information

Additional Description:

Since opening a 1,200 sqm production and laboratory facility in 2017, piCHEM has manufactured peptides in line with ICH guidelines at facilities inspected and approved by national authorities and the US FDA. Its contract manufacturing team supports drug development through all clinical trial phases, producing GMP APIs from milligram to several-hundred-gram scale using techniques from conventional solution-phase synthesis to solid-phase peptide synthesis (SPPS), with reversed-phase and ion-exchange chromatography applied as standard purification methods.
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