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Esco Aster

End-to-end bioinnovation from concept to commercial production with GMP-compliant manufacturing and clinical development.

Esco Aster is a vertically integrated CDMO and CRO delivering end-to-end contract solutions from process development and GMP manufacturing through clinical research, with specialized capabilities in vaccine production, cell therapy, plasmid DNA, extracellular vesicles, and GLP toxicology.

Phases

Indications / Therapeutic Areas

Services

Modalities

Technical specifications & accreditations

About this organization

Overview

Esco Aster is a vertically integrated bioinnovation venture accelerator and contract research and manufacturing organization (CRDMO) delivering end-to-end "idea-to-exit" solutions spanning consultancy, research, CMC development, manufacturing, testing, clinical development, and strategic capital support.

Core Capabilities

Manufacturing & Process Development

  • cGMP-compliant vaccine development and manufacturing with single-use solutions, process scale-up/scale-down, and process validation
  • Cell bank preservation for cell lines, microbial cells, and biologics
  • Cell culture process development and optimization, including medium optimization and seed preparation
  • Plasmid DNA manufacturing at preclinical, clinical, and commercial scales with GMP standards
  • Aseptic fill-and-finish services (first in Southeast Asia/ASEAN) with USP <1207> container-closure integrity testing and in-house autoclave sterilization
  • Advanced formulation solutions for inhalation-based exosome delivery (nasal spray, nebulizer, dry powder)

Therapeutic Modalities

  • Vaccine technologies (conventional inactivated, attenuated live, subunit, VLPs, DNA, self-amplifying RNA)
  • Cell therapy including CAR-T cells, CAR-NK cells, and CAR-dendritic cells with process design through GMP manufacture
  • Extracellular vesicles and exosome therapeutics
  • Adherent cell line creation, banking, characterization, and storage
  • Plasmid DNA for gene therapy applications

Preclinical & Clinical Services

  • GLP Toxicology studies (material production and study oversight) aligned with investment milestones
  • Preclinical to clinical testing for drug efficacy determination
  • Lead optimization through commercialization support for advanced therapies
  • MiniTide® 3D tissue culture platform as parallel to traditional 2D and organoid approaches

Strategic Services

  • Strategic capital support and fundraising services
  • Business development and enterprise support
  • Venture ecosystem partnership

Therapeutic Areas

Serves diagnostics, therapeutics, vaccines, dermatology, dermocosmetics, cosmeceuticals, medical aesthetics, injectables, coatings, nutraceuticals, and cellular agriculture. Demonstrated commercial deployment in human and animal vaccines, dermocosmetics, cell-based nutrition, and clinical-grade stem cells and exosomes.

Certifications

AuthorityIdentifierSource
cGMPcGMP-compliantView
GLPGLP ToxicologyView

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