Focuses on solid-state R&D, including polymorph, salt, and cocrystal screening, crystallization process development, and structural characterization using complementary techniques.
Disclosed in the official company history, with year-level precision only; this does not establish that there was no subsequent financing by the access date.
Profile review: 2026-11-04 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.
Disease tags match recorded text mentions and require program-level verification.
Technology, programs & evidence
The group connects candidates with clinical and commercial supply through solid-state, preformulation, oral formulation development, and manufacturing services. Formulation execution entities include CFS and Candoo.
The solid-form screening service page explicitly lists polymorph, salt, and cocrystal screening.
Disclosed structural characterization methods include XRPD, ssNMR, SCXRD, and MicroED. Complementary techniques should be selected for each project.
The current website lists MicroED, XRPD, ssNMR, and SCXRD as structural characterization services.
An April 2026 collaboration announcement with ELDICO disclosed plans to introduce a dedicated ED-1 in Suzhou. The announcement alone does not establish completed acceptance testing.
Program / service
Target / indication
Representative stage
Evidence & scope
Formulation development / contract manufacturing capabilities
Defined by the client project · Defined by the client project
Services / platform
Service pages do not establish human evidence for every project
Solid-state R&D capabilities
Determined by the submitted sample and research question · Not applicable; service capability
Services / platform
Not applicable; not a human clinical program
MicroED / 3D ED service capabilities
Determined by the submitted sample and research question · Not applicable; service capability
Services / platform
Not applicable; not a human clinical program
Related news & literature
Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.
Biotech Assistant · Original commentary · Blog / commentary
This article explores how Microcrystal Electron Diffraction (MicroED) is set to revolutionize drug polymorph research workflows. Drawing upon recent news, official websites, and LinkedIn updates from Crystal Pharmatech and Eldico, it clearly distinguishes between verified facts, industry viewpoints, and information pending verification.
Crystal Pharmatech’s November 4 announcement confirms ED-1 service in Suzhou. Its service page describes integration with solid-form screening for small crystals and pharmaceutical solid forms.
A Nature Communications study reports a peptide–oligonucleotide nanohybrid for bone-targeted miR-26a-5p delivery. The original abstract describes reduced GSK-3β expression and stabilization of HIF-1α, supporting coupled bone formation and angiogenesis. Systemic administration limited skeletal and vascular injury in a rat glucocorticoid-induced bone-loss model. This is preclinical miRNA delivery, not oral cyclic peptide therapy or human efficacy evidence.
FDA granted accelerated approval to amivantamab and hyaluronidase-lpuj for adults with recurrent or metastatic head and neck squamous cell carcinoma after platinum chemotherapy and an anti-PD-(L)1 antibody. HPV-associated oropharyngeal cancer is excluded. In the 102-patient OrigAMI-4 efficacy population, response rate was 42%. Continued approval requires confirmatory clinical benefit; this is not traditional full approval.
Phillips Medisize announced an investment to acquire the complete footprint of its Chippenham site in England, strengthening its Global Inhalation Center of Excellence alongside Cambridge. Building on the 2025 Vectura acquisition, the site supports drug-device formulation development and early- and late-stage clinical supplies. The announcement links the investment to anticipated growth in complex inhaled therapies.
Research this company together
Discussions are for signed-in members. Personal notes remain separate from company research.
Available capacity, site-specific qualifications, project delivery history, pricing, and technology transfer terms require confirmation with the execution entity.
Company service pages support the stated scope but do not establish clinical validation of every dosage form or client program.
The group, subsidiary, and execution site should be confirmed separately before project initiation and contracting. They should not be counted as three independent groups.
Public sources confirm service availability. Sample suitability, scope of work, pricing, turnaround time, success criteria, and the quality system require direct confirmation.
This record describes service capabilities, not the clinical progress of a drug candidate or an independent validation of service success rates.
The website confirms commercial MicroED services. The ED-1 commissioning and acceptance dates, execution site, criteria for absolute configuration assignment, and quality system require direct confirmation.
This record covers small molecules and pharmaceutical solid-state analysis. General cryo-EM protein analysis is not treated as evidence of protein MicroED.